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Randomized Clinical Trial of Rib Fixation Versus Medical Analgesia in Uncomplicated Rib Fractures on Pain Control. (PAROS)

Primary Purpose

Rib Fractures

Status
Recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Rib fixation
Analgesia
Sponsored by
Benoît Bédat
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rib Fractures focused on measuring thoracic trauma, rib fixation, medical device

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • At least 2 rib fractures
  • At least 1 dislocated rib fracture
  • Fractures accessible to surgery
  • Thoracic trauma no more than two days prior to screening for inclusion
  • Thoracic epidural analgesia
  • Written informed consent

Exclusion Criteria:

  • Any other concomitant fractures excepted clavicle fracture
  • Respiratory distress syndrome according to the Berlin definition
  • Presence of >1.5 liter of blood drained from the pleural space
  • Hemostasis disorder defined by any of the following criteria:

    • Platelet count < 70'000/mm3,
    • International Normalized Ratio (INR) > 1.2 (Prothrombin < 70%)
    • activated partial thromboplastin time (aPTT) ≥ 60 seconds
    • drugs such as: P2Y12 antagonists (clopidogrel, prasugrel) and glycoprotein IIb/IIIa antagonists (abciximab, tirofiban)
  • Pathological rib fracture due to metastasis
  • Hemodynamic instability: systolic blood pressure < 100 mmHg and heart rate > 100 beats per minute
  • Neurologic disorder: Glasgow Coma Score < 13 in the initial 24 hours, or intracerebral, epidural, subdural, or subarachnoid hemorrhages, or cerebral contusion
  • Titanium allergy
  • Known or suspected non-compliance to medical therapy due to drug or alcohol abuse
  • Age <18 years old
  • Women who know they are pregnant or breast feeding
  • Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc.

Sites / Locations

  • Unit of Thoracic and Endocrine Surgery, University Hospitals of GenevaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Rib fixation (medical devices)

Pain medication (comparator treatment)

Arm Description

Surgery and pain medication. The pain of patients will be treated with rib fixation and pain medication.

Pain medication only.

Outcomes

Primary Outcome Measures

Pain severity
Pain level reported by the participant, as assessed via the first part of the French version of the brief pain inventory (BPI) questionnaire. 0-10 scale. 10 indicating worst pain

Secondary Outcome Measures

Pain severity
Pain level reported by the participant, as assessed via the first part of the French version of the brief pain inventory (BPI) questionnaire. 0-10 scale. 10 indicating worst pain
Pain severity
Pain level reported by the participant, as assessed via the first part of the French version of the brief pain inventory (BPI) questionnaire. 0-10 scale. 10 indicating worst pain
Pain severity
Pain level reported by the participant, as assessed via the first part of the French version of the brief pain inventory (BPI) questionnaire. 0-10 scale. 10 indicating worst pain
Pain severity
Pain level reported by the participant, as assessed via the first part of the French version of the brief pain inventory (BPI) questionnaire. 0-10 scale. 10 indicating worst pain
Pain severity
Pain level reported by the participant, as assessed via the first part of the French version of the brief pain inventory (BPI) questionnaire. 0-10 scale. 10 indicating worst pain
Anxiety and Depression.
hospital anxiety and depression scale (HADS). Score 0-21. 21 = severe depression or anxiety
Anxiety and Depression.
hospital anxiety and depression scale (HADS). Score 0-21. 21 = severe depression or anxiety
Anxiety and Depression.
hospital anxiety and depression scale (HADS). Score 0-21. 21 = severe depression or anxiety
Neuropathic pain
The French questionnaire "Douleur Neuropathique en 4 Questions (DN4)" is completed by an investigator during follow-up visits. The DN4 questionnaire was developed to diagnose polyneuropathy. Three items are linked with neuropathic pain examination, and seven items to pain symptoms. Score 0-10. Score >4 indicates neuropathic pain.
Neuropathic pain
The French questionnaire "Douleur Neuropathique en 4 Questions (DN4)" is completed by an investigator during follow-up visits. The DN4 questionnaire was developed to diagnose polyneuropathy. Three items are linked with neuropathic pain examination, and seven items to pain symptoms. Score 0-10. Score >4 indicates neuropathic pain.
Pain interference
The last items of the BPI questionnaires measure how much pain has interfered with seven daily activities, including general activity, walking, work, mood, enjoyment of life, relations with others and sleep. BPI pain interference is scored as the mean of the seven items. Score 0-10. 10 = high interference of pain with activities.
Pain interference
The last items of the BPI questionnaires measure how much pain has interfered with seven daily activities, including general activity, walking, work, mood, enjoyment of life, relations with others and sleep. BPI pain interference is scored as the mean of the seven items. Score 0-10. 10 = high interference of pain with activities.
Pain interference
The last items of the BPI questionnaires measure how much pain has interfered with seven daily activities, including general activity, walking, work, mood, enjoyment of life, relations with others and sleep. BPI pain interference is scored as the mean of the seven items. Score 0-10. 10 = high interference of pain with activities.
Pain interference
The last items of the BPI questionnaires measure how much pain has interfered with seven daily activities, including general activity, walking, work, mood, enjoyment of life, relations with others and sleep. BPI pain interference is scored as the mean of the seven items. Score 0-10. 10 = high interference of pain with activities.
Pain interference
The last items of the BPI questionnaires measure how much pain has interfered with seven daily activities, including general activity, walking, work, mood, enjoyment of life, relations with others and sleep. BPI pain interference is scored as the mean of the seven items. Score 0-10. 10 = high interference of pain with activities.
Pain interference
The last items of the BPI questionnaires measure how much pain has interfered with seven daily activities, including general activity, walking, work, mood, enjoyment of life, relations with others and sleep. BPI pain interference is scored as the mean of the seven items. Score 0-10. 10 = high interference of pain with activities.
Health and well being
The 36-Item Health Survey (SF-36) taps eight health concepts: physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue, and general health perceptions. Score: 0-100. 100 = better functioning
Health and well being
The 36-Item Health Survey (SF-36) taps eight health concepts: physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue, and general health perceptions. Score: 0-100. 100 = better functioning
Health and well being
The 36-Item Health Survey (SF-36) taps eight health concepts: physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue, and general health perceptions. Score: 0-100. 100 = better functioning
Analgesic medication during hospitalisation
During hospitalization, each day since the enrolment, amount and type of analgesic medication are recorded from the computerized patient record system.
Analgesic medication at home
After discharge, analgesic medication (type and amount) is tracked using a custom questionnaire.
Analgesic medication at home
After discharge, analgesic medication (type and amount) is tracked using a custom questionnaire.
Analgesic medication at home
After discharge, analgesic medication (type and amount) is tracked using a custom questionnaire.
Analgesic medication at home
After discharge, analgesic medication (type and amount) is tracked using a custom questionnaire.
Analgesic medication at home
After discharge, analgesic medication (type and amount) is tracked using a custom questionnaire.
Productivity & return to work
The work productivity and activity impairment (WPAI) questionnaire is used. It assesses impairments in both paid work and unpaid work. It measures absenteeism, presenteeism as well as the impairments in unpaid activity because of health problem during the past seven days. Score 0-10. 10 = high impairment
Productivity & return to work
The work productivity and activity impairment (WPAI) questionnaire is used. It assesses impairments in both paid work and unpaid work. It measures absenteeism, presenteeism as well as the impairments in unpaid activity because of health problem during the past seven days. Score 0-10. 10 = high impairment
Productivity & return to work
The work productivity and activity impairment (WPAI) questionnaire is used. It assesses impairments in both paid work and unpaid work. It measures absenteeism, presenteeism as well as the impairments in unpaid activity because of health problem during the past seven days. Score 0-10. 10 = high impairment
Productivity & return to work
The work productivity and activity impairment (WPAI) questionnaire is used. It assesses impairments in both paid work and unpaid work. It measures absenteeism, presenteeism as well as the impairments in unpaid activity because of health problem during the past seven days. Score 0-10. 10 = high impairment
Productivity & return to work
The work productivity and activity impairment (WPAI) questionnaire is used. It assesses impairments in both paid work and unpaid work. It measures absenteeism, presenteeism as well as the impairments in unpaid activity because of health problem during the past seven days. Score 0-10. 10 = high impairment
Pulmonary function
Forced vital capacity (FVC, % predicted) measured according to the recommendations of the European Respiratory Society. The best value of at least three tests is recorded.
Pulmonary function, forced vital capacity
Forced vital capacity (FVC, % predicted) measured according to the recommendations of the European Respiratory Society. The best value of at least three tests is recorded.
Pulmonary function, peak expiratory flow
Peak expiratory flow (PEF, L/min) measured according to the recommendations of the European Respiratory Society. The best value of at least three tests is recorded.
Pulmonary function, peak expiratory flow
Peak expiratory flow (PEF, L/min) measured according to the recommendations of the European Respiratory Society. The best value of at least three tests is recorded.
Pulmonary function, sniff nasal inspiratory pressure
sniff nasal inspiratory pressure (in in cmH2O) measured according to the recommendations of the European Respiratory Society. The best value of at least three tests is recorded.
Pulmonary function, sniff nasal inspiratory pressure
sniff nasal inspiratory pressure (in in cmH2O) measured according to the recommendations of the European Respiratory Society. The best value of at least three tests is recorded.
Pulmonary function, inspiratory pressure
Maximum inspiratory pressure (in in cmH2O) measured according to the recommendations of the European Respiratory Society. The best value of at least three tests is recorded.
Pulmonary function, inspiratory pressure
Maximum inspiratory pressure (in in cmH2O) measured according to the recommendations of the European Respiratory Society. The best value of at least three tests is recorded.
Length of hospital stay
Length of hospital stay is reported in days from the day of hospitalization until the hospital discharge. The length of convalescence stay is also reported.
Total costs
Costs are reported at the end of the follow-up period (12 months) in swiss francs. They include costs for hospital treatment and costs for medication.
Adverse events
We collect safety outcomes in accordance with international standards (ISO 14155 and ICH-GCP)

Full Information

First Posted
December 6, 2020
Last Updated
May 17, 2022
Sponsor
Benoît Bédat
Collaborators
Centre Hospitalier Universitaire Vaudois, Hôpital du Valais
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1. Study Identification

Unique Protocol Identification Number
NCT04745520
Brief Title
Randomized Clinical Trial of Rib Fixation Versus Medical Analgesia in Uncomplicated Rib Fractures on Pain Control.
Acronym
PAROS
Official Title
Comparison of Rib Fixation With Medical Analgesia in Patients With Uncomplicated Rib Fractures on Pain Control: a Multi-center Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 12, 2021 (Actual)
Primary Completion Date
March 2023 (Anticipated)
Study Completion Date
March 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Benoît Bédat
Collaborators
Centre Hospitalier Universitaire Vaudois, Hôpital du Valais

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Uncomplicated costal fractures often result in persistent pain over the long term. Indeed, cohort studies showed that at 6 months, 22% of patients still had pain and 56% had functional disability. The impact of costal fractures on quality of life is underestimated. The socio-psycho-economic consequences are substantial. Previous studies have shown that an important factor for persistent pain and functional disability is the intensity of the initial pain. However, preliminary studies have shown promising results with surgical fixation of rib fractures: reduced need for analgesic drugs, reduced pain at 1 month, reduced complications and improved motor skills in patients over 65 years of age. To date, the only clinical trials that exist focused on the fixation of complicated rib dislocations. While fixation of uncomplicated rib fractures is a common practice, no randomized studies have been conducted to evaluate its impact on pain and quality of life in the medium and long term. In this context, the aim of our randomized study is to compare pain at 2 months between operated and non-operated patients with uncomplicated rib fractures.
Detailed Description
Background. Until recently, functional disability and chronic pain and following uncomplicated rib fractures have been scarcely studied. Studies described persistent pain and disability in, respectively, 59% and 76% of patients at two months, and in 22% and 53% of patients at 6 months. In a retrospective study including 216 patients with an isolated thoracic injury, only 34.2% of patients had a good recovery at one year and the six-month return to work rate is of 63%. Persistent pain and disability following rib fractures therefore result in a large psycho-socio-economic impact for health-care system. The only predictive factor for persistent pain and disability is the pain intensity within the first few days after injury. Similarly, the intensity of pain within the first days after thoracotomy predicts long-term post-thoracotomy pain. In a recent meta-analysis, epidural analgesia provides better acute pain relief than intravenous, paravertebral, and intercostal interventions. While meta-analyses conclude that operative fixation of complicated flail chest provide better outcome, the impact of surgery on pain in uncomplicated rib fracture is seldom studied. Some retrospective studies showed promising results of rib fixation with surgery in patients with uncomplicated rib fractures: A study showed that rib fixation reduced postoperative analgesic requirements. Similarly, another study showed that pain was significantly reduced one month after surgery as compared to a non-surgical approach. Finally, it has been recently observed a decreased mortality and respiratory complications after surgery in patients over 65 years old as well as a better functional status at two weeks, two months, and four months. Trial objectives. No previous studies have provided definitive evidence for recommending rib fixation over simple pain medication to control pain. Our hypothesis is that a surgical approach may have further benefits as compared to a conservative treatment. The primary objective of the study is to compare pain two months after injury between two groups: group 1) patients who are treated with surgery and analgesic treatment; and group 2) patients who are treated with analgesic treatment alone. The secondary objective is to perform a longitudinal analysis over one year of the following parameters: amount of pain medication, quality of life, anxiety and depression, pulmonary capacity, return to work, and adverse events. Financial aspects are also investigated.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rib Fractures
Keywords
thoracic trauma, rib fixation, medical device

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This pragmatic trial is a multi-center, two-arm, parallel-group, superiority randomized-controlled trial.
Masking
None (Open Label)
Masking Description
it is not possible to blind the patients and investigators regarding surgery.
Allocation
Randomized
Enrollment
102 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Rib fixation (medical devices)
Arm Type
Experimental
Arm Description
Surgery and pain medication. The pain of patients will be treated with rib fixation and pain medication.
Arm Title
Pain medication (comparator treatment)
Arm Type
Active Comparator
Arm Description
Pain medication only.
Intervention Type
Device
Intervention Name(s)
Rib fixation
Intervention Description
Rib fixation is performed by a senior surgeon. The patient is under general anesthesia. A thoracotomy focused on the fracture is performed to optimize access to the rib to be repaired. Video-assisted thoracic surgery (VATS) can be performed to better localize rib fractures. Significant muscle division is avoided. Removal of the periosteum is not required. The broken rib segments are approximated with forceps and the medical devices are used to fix the fracture. The medical devices are implemented according to the manufacturers' recommendations. The goal is to stabilize the chest wall. It is not useful to fix all fractures to stabilize the wall. A chest tube can be placed at the end of the operation. Medical devices The following medical devices can be used: MatrixRIB™, De Puy Synthes Companies, Zuchwill, Switzerland STRATOS™, MedXpert GmbH, Heitersheim, Germany NiTi Fixing PlatesTM, IAWAI, Yandzhou, China
Intervention Type
Drug
Intervention Name(s)
Analgesia
Intervention Description
Epidural analgesia is continuing for 24 to 72 hours post-randomization to maximize outcome benefits. Afterwards, paracetamol, NSAID and/or opioid treatment are used according to pain severity. In case of opioid use, morphine treatment is preferred. However, other opioid drugs or doses can be considered to better customize the treatment.
Primary Outcome Measure Information:
Title
Pain severity
Description
Pain level reported by the participant, as assessed via the first part of the French version of the brief pain inventory (BPI) questionnaire. 0-10 scale. 10 indicating worst pain
Time Frame
Two months after injury
Secondary Outcome Measure Information:
Title
Pain severity
Description
Pain level reported by the participant, as assessed via the first part of the French version of the brief pain inventory (BPI) questionnaire. 0-10 scale. 10 indicating worst pain
Time Frame
At recruitment (baseline)
Title
Pain severity
Description
Pain level reported by the participant, as assessed via the first part of the French version of the brief pain inventory (BPI) questionnaire. 0-10 scale. 10 indicating worst pain
Time Frame
One month after injury
Title
Pain severity
Description
Pain level reported by the participant, as assessed via the first part of the French version of the brief pain inventory (BPI) questionnaire. 0-10 scale. 10 indicating worst pain
Time Frame
Three months after injury
Title
Pain severity
Description
Pain level reported by the participant, as assessed via the first part of the French version of the brief pain inventory (BPI) questionnaire. 0-10 scale. 10 indicating worst pain
Time Frame
Six months after injury
Title
Pain severity
Description
Pain level reported by the participant, as assessed via the first part of the French version of the brief pain inventory (BPI) questionnaire. 0-10 scale. 10 indicating worst pain
Time Frame
Twelve months after injury
Title
Anxiety and Depression.
Description
hospital anxiety and depression scale (HADS). Score 0-21. 21 = severe depression or anxiety
Time Frame
At recruitment (baseline)
Title
Anxiety and Depression.
Description
hospital anxiety and depression scale (HADS). Score 0-21. 21 = severe depression or anxiety
Time Frame
One month after injury
Title
Anxiety and Depression.
Description
hospital anxiety and depression scale (HADS). Score 0-21. 21 = severe depression or anxiety
Time Frame
Two months after injury
Title
Neuropathic pain
Description
The French questionnaire "Douleur Neuropathique en 4 Questions (DN4)" is completed by an investigator during follow-up visits. The DN4 questionnaire was developed to diagnose polyneuropathy. Three items are linked with neuropathic pain examination, and seven items to pain symptoms. Score 0-10. Score >4 indicates neuropathic pain.
Time Frame
Two months after injury
Title
Neuropathic pain
Description
The French questionnaire "Douleur Neuropathique en 4 Questions (DN4)" is completed by an investigator during follow-up visits. The DN4 questionnaire was developed to diagnose polyneuropathy. Three items are linked with neuropathic pain examination, and seven items to pain symptoms. Score 0-10. Score >4 indicates neuropathic pain.
Time Frame
Six months after injury
Title
Pain interference
Description
The last items of the BPI questionnaires measure how much pain has interfered with seven daily activities, including general activity, walking, work, mood, enjoyment of life, relations with others and sleep. BPI pain interference is scored as the mean of the seven items. Score 0-10. 10 = high interference of pain with activities.
Time Frame
At recruitment (baseline)
Title
Pain interference
Description
The last items of the BPI questionnaires measure how much pain has interfered with seven daily activities, including general activity, walking, work, mood, enjoyment of life, relations with others and sleep. BPI pain interference is scored as the mean of the seven items. Score 0-10. 10 = high interference of pain with activities.
Time Frame
One month after injury
Title
Pain interference
Description
The last items of the BPI questionnaires measure how much pain has interfered with seven daily activities, including general activity, walking, work, mood, enjoyment of life, relations with others and sleep. BPI pain interference is scored as the mean of the seven items. Score 0-10. 10 = high interference of pain with activities.
Time Frame
Two months after injury
Title
Pain interference
Description
The last items of the BPI questionnaires measure how much pain has interfered with seven daily activities, including general activity, walking, work, mood, enjoyment of life, relations with others and sleep. BPI pain interference is scored as the mean of the seven items. Score 0-10. 10 = high interference of pain with activities.
Time Frame
Three months after injury
Title
Pain interference
Description
The last items of the BPI questionnaires measure how much pain has interfered with seven daily activities, including general activity, walking, work, mood, enjoyment of life, relations with others and sleep. BPI pain interference is scored as the mean of the seven items. Score 0-10. 10 = high interference of pain with activities.
Time Frame
Six months after injury
Title
Pain interference
Description
The last items of the BPI questionnaires measure how much pain has interfered with seven daily activities, including general activity, walking, work, mood, enjoyment of life, relations with others and sleep. BPI pain interference is scored as the mean of the seven items. Score 0-10. 10 = high interference of pain with activities.
Time Frame
Twelve months after injury
Title
Health and well being
Description
The 36-Item Health Survey (SF-36) taps eight health concepts: physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue, and general health perceptions. Score: 0-100. 100 = better functioning
Time Frame
At recruitment (baseline)
Title
Health and well being
Description
The 36-Item Health Survey (SF-36) taps eight health concepts: physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue, and general health perceptions. Score: 0-100. 100 = better functioning
Time Frame
Two months after injury
Title
Health and well being
Description
The 36-Item Health Survey (SF-36) taps eight health concepts: physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue, and general health perceptions. Score: 0-100. 100 = better functioning
Time Frame
Six months after injury
Title
Analgesic medication during hospitalisation
Description
During hospitalization, each day since the enrolment, amount and type of analgesic medication are recorded from the computerized patient record system.
Time Frame
At recruitement (baseline)
Title
Analgesic medication at home
Description
After discharge, analgesic medication (type and amount) is tracked using a custom questionnaire.
Time Frame
One month after injury
Title
Analgesic medication at home
Description
After discharge, analgesic medication (type and amount) is tracked using a custom questionnaire.
Time Frame
Two months after injury
Title
Analgesic medication at home
Description
After discharge, analgesic medication (type and amount) is tracked using a custom questionnaire.
Time Frame
Three months after injury
Title
Analgesic medication at home
Description
After discharge, analgesic medication (type and amount) is tracked using a custom questionnaire.
Time Frame
Six months after injury
Title
Analgesic medication at home
Description
After discharge, analgesic medication (type and amount) is tracked using a custom questionnaire.
Time Frame
Twelve months after injury
Title
Productivity & return to work
Description
The work productivity and activity impairment (WPAI) questionnaire is used. It assesses impairments in both paid work and unpaid work. It measures absenteeism, presenteeism as well as the impairments in unpaid activity because of health problem during the past seven days. Score 0-10. 10 = high impairment
Time Frame
One month after injury
Title
Productivity & return to work
Description
The work productivity and activity impairment (WPAI) questionnaire is used. It assesses impairments in both paid work and unpaid work. It measures absenteeism, presenteeism as well as the impairments in unpaid activity because of health problem during the past seven days. Score 0-10. 10 = high impairment
Time Frame
Two months after injury
Title
Productivity & return to work
Description
The work productivity and activity impairment (WPAI) questionnaire is used. It assesses impairments in both paid work and unpaid work. It measures absenteeism, presenteeism as well as the impairments in unpaid activity because of health problem during the past seven days. Score 0-10. 10 = high impairment
Time Frame
Three months after injury
Title
Productivity & return to work
Description
The work productivity and activity impairment (WPAI) questionnaire is used. It assesses impairments in both paid work and unpaid work. It measures absenteeism, presenteeism as well as the impairments in unpaid activity because of health problem during the past seven days. Score 0-10. 10 = high impairment
Time Frame
Six months after injury
Title
Productivity & return to work
Description
The work productivity and activity impairment (WPAI) questionnaire is used. It assesses impairments in both paid work and unpaid work. It measures absenteeism, presenteeism as well as the impairments in unpaid activity because of health problem during the past seven days. Score 0-10. 10 = high impairment
Time Frame
Twelve months after injury
Title
Pulmonary function
Description
Forced vital capacity (FVC, % predicted) measured according to the recommendations of the European Respiratory Society. The best value of at least three tests is recorded.
Time Frame
Two months after injury
Title
Pulmonary function, forced vital capacity
Description
Forced vital capacity (FVC, % predicted) measured according to the recommendations of the European Respiratory Society. The best value of at least three tests is recorded.
Time Frame
Six months after injury
Title
Pulmonary function, peak expiratory flow
Description
Peak expiratory flow (PEF, L/min) measured according to the recommendations of the European Respiratory Society. The best value of at least three tests is recorded.
Time Frame
Two months after injury
Title
Pulmonary function, peak expiratory flow
Description
Peak expiratory flow (PEF, L/min) measured according to the recommendations of the European Respiratory Society. The best value of at least three tests is recorded.
Time Frame
Six months after injury
Title
Pulmonary function, sniff nasal inspiratory pressure
Description
sniff nasal inspiratory pressure (in in cmH2O) measured according to the recommendations of the European Respiratory Society. The best value of at least three tests is recorded.
Time Frame
Two months after injury
Title
Pulmonary function, sniff nasal inspiratory pressure
Description
sniff nasal inspiratory pressure (in in cmH2O) measured according to the recommendations of the European Respiratory Society. The best value of at least three tests is recorded.
Time Frame
Six months after injury
Title
Pulmonary function, inspiratory pressure
Description
Maximum inspiratory pressure (in in cmH2O) measured according to the recommendations of the European Respiratory Society. The best value of at least three tests is recorded.
Time Frame
Two months after injury
Title
Pulmonary function, inspiratory pressure
Description
Maximum inspiratory pressure (in in cmH2O) measured according to the recommendations of the European Respiratory Society. The best value of at least three tests is recorded.
Time Frame
Six months after injury
Title
Length of hospital stay
Description
Length of hospital stay is reported in days from the day of hospitalization until the hospital discharge. The length of convalescence stay is also reported.
Time Frame
from admission to discharge, up to four weeks
Title
Total costs
Description
Costs are reported at the end of the follow-up period (12 months) in swiss francs. They include costs for hospital treatment and costs for medication.
Time Frame
Twelve months after injury
Title
Adverse events
Description
We collect safety outcomes in accordance with international standards (ISO 14155 and ICH-GCP)
Time Frame
From inclusion to the end of the study, up to 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: At least 2 rib fractures At least 1 dislocated rib fracture Fractures accessible to surgery Thoracic trauma no more than two days prior to screening for inclusion Thoracic epidural analgesia Written informed consent Exclusion Criteria: Any other concomitant fractures excepted clavicle fracture Respiratory distress syndrome according to the Berlin definition Presence of >1.5 liter of blood drained from the pleural space Hemostasis disorder defined by any of the following criteria: Platelet count < 70'000/mm3, International Normalized Ratio (INR) > 1.2 (Prothrombin < 70%) activated partial thromboplastin time (aPTT) ≥ 60 seconds drugs such as: P2Y12 antagonists (clopidogrel, prasugrel) and glycoprotein IIb/IIIa antagonists (abciximab, tirofiban) Pathological rib fracture due to metastasis Hemodynamic instability: systolic blood pressure < 100 mmHg and heart rate > 100 beats per minute Neurologic disorder: Glasgow Coma Score < 13 in the initial 24 hours, or intracerebral, epidural, subdural, or subarachnoid hemorrhages, or cerebral contusion Titanium allergy Known or suspected non-compliance to medical therapy due to drug or alcohol abuse Age <18 years old Women who know they are pregnant or breast feeding Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Benoît Bédat, MD
Phone
+41795904475
Email
benoit.bedat@hcuge.ch
First Name & Middle Initial & Last Name or Official Title & Degree
Philippe Terrier, PhD
Phone
+41763906178
Email
ph.terrier@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Benoît Bédat, MD
Organizational Affiliation
Hôpitaux universitaires de Genève
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Frédéric Triponez, Prof.
Organizational Affiliation
Hôpitaux universitaires de Genève
Official's Role
Study Chair
Facility Information:
Facility Name
Unit of Thoracic and Endocrine Surgery, University Hospitals of Geneva
City
Geneva
ZIP/Postal Code
1205
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Principal Investigator
Email
Benoit.Bedat@hcuge.ch
First Name & Middle Initial & Last Name & Degree
Clinical Research Associate
Email
ph.terrier@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
12813323
Citation
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Randomized Clinical Trial of Rib Fixation Versus Medical Analgesia in Uncomplicated Rib Fractures on Pain Control.

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