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The Pain Control in Rib Fracture With Non-invasive Stabilization (RCT)

Primary Purpose

Rib Fractures, Pain, Thorax; Fracture

Status
Unknown status
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Posthorax Thoraxbelt
Sponsored by
National Taiwan University Hospital Hsin-Chu Branch
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Rib Fractures focused on measuring Rib fractures, pain control, Posthorax Thoraxbelt

Eligibility Criteria

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

Inclusion Criteria:

  • The adult patients with rib fractures (inpatients/outpatients)
  • The patients will be assessed to the further admission (inpatients)
  • The patients will be assessed to be at follow-up clinic visit (outpatients)

Exclusion Criteria:

  • The accident of rib fractures has been occurred over 24 hours. (inpatients/outpatients)
  • Refuse to be arranged to the admission (inpatients)
  • Refuse to receive the CT scan (inpatients/outpatients)
  • Chest wall infection or other diseases (inpatients/outpatients)
  • Chest wall infected by rumors (inpatients/outpatients)
  • Pregnancy (inpatients/outpatients)
  • Further complications arise (inpatients/outpatients)
  • Known allergy to ThoraxBelt (inpatients/outpatients)

Sites / Locations

  • National Taiwan University Hospital Hsin-Chu BranchRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

No Intervention

Experimental

No Intervention

Arm Label

ThoraxBelt (Inpatients)

Standard Care (Inpatients)

ThoraxBelt (Outpatients)

Standard Care (Outpatients)

Arm Description

Received ThoraxBelt after the surgery in addition to oral analgesics. Standard care for pain management will be the same as the Standard Care Arm (Inpatients).

Standard Care with IV PCA and on-request oral painkiller.

Received ThoraxBelt at the emergency room in addition to oral analgesics. Standard care for pain management will be the same as the Standard Care Arm (Outpatients).

Standard Care and on-request oral painkiller.

Outcomes

Primary Outcome Measures

Inpatients: Visual analog scale (VAS)
A pain score will be assessed to each patient after the total amount of visual analog scale. The minimum is 0 and the maximum is 10, from the least pain to the highest pain.
Outpatients: Visual analog scale (VAS)
A pain score will be assessed to each patient after the total amount of visual analog scale. The minimum is 0 and the maximum is 10, from the l

Secondary Outcome Measures

Inpatients: IV PCA dose
the accumulated IV PCA drug dose
Inpatients: On-request oral painkiller dose
the accumulated oral painkiller dose
Inpatients: Complication during the hospital stay
Any complications whether related to ThoraxBelt or not
Inpatients: Length of hospital stay
the amount of days in hospital stay
Inpatients: VAS before discharge
Visual analog scale before discharge
Inpatients: The amount of unanticipated events
send to the ICU admission, a second surgery or death
Inpatients: VAS in outpatient clinic follow-up
VAS during the 1-week, 1-month and 3-month outpatient clinic visit after the surgery
Inpatients/Outpatients: X-ray examination
An X-ray examination at an outpatient clinic
Inpatients/Outpatients: Compliance on ThoraxBelt after discharge
How long is the ThroaxBelt removed except during the bath within the whole day. The unit is hour.
Outpatients: Complication during the follow-up period
Any complications whether related to ThoraxBelt or not
Outpatients: The amount of unanticipated events
send to the ward admission, ICU admission, a surgery or OHCA

Full Information

First Posted
October 4, 2021
Last Updated
July 17, 2022
Sponsor
National Taiwan University Hospital Hsin-Chu Branch
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1. Study Identification

Unique Protocol Identification Number
NCT05080686
Brief Title
The Pain Control in Rib Fracture With Non-invasive Stabilization (RCT)
Official Title
The Management and Assessment of Pain Control in Rib Fracture With Non-invasive Stabilization: a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2022 (Actual)
Primary Completion Date
December 31, 2022 (Anticipated)
Study Completion Date
December 31, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Taiwan University Hospital Hsin-Chu Branch

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Brief summary: Background: Rib fractures are one of the most common causes of trauma disabilities and have become an important health issue. Patients usually suffer from severe pain. A rapid and adequate pain control is considered as a priority to improve respiratory mechanics and reduce the risk of pulmonary and systemic complications. So far, there was no gold standard regarding pain control for rib fractures. Objective: To assess the effect of the newly-designed Prosthorax Thoraxbelt in addition to oral analgesics on pain control of rib fractures Method: There will be two groups of patients in this study. One group will be the patients with rib fractures who are necessary for in-hospital intense pain control. The other will consist of follow-up patients with rib fractures at an outpatient clinic. The investigators will aim to recruit 30 and 82 patients respectively.
Detailed Description
The study has been approved by the hospital research ethics committee. Arm1: The management and assessment of pain control in rib fracture with non-invasive stabilization: a randomized controlled trial (inpatients) Arm2: The management and assessment of pain control in rib fracture with non-invasive stabilization: a randomized controlled trial (outpatients) Primary outcome: inpatient: Visual analog scale (VAS) for 6 hours, 12 hours and 24 hours after the surgery outpatient: Visual analog scale (VAS) for the times at emergency room; 3 days, 3 weeks and 3 months after rib fracture at an outpatient clinic. Secondary outcome: inpatients The accumulated dose of the inter-venous patient-controlled analgesic drug within 6 hours, 24 hours and 48 hours after the surgery Complication during the hospital stay Hospital stay VAS before discharge Unanticipated events (ICU admission, a second surgery, death) VAS during the 1-week, 1-month and 3-month outpatient clinic visit after the surgery An X-ray examination at an outpatient clinic Compliance on ThoraxBelt after discharge outpatients Complication during the follow-up period Unanticipated events (ward admission, ICU admission, a surgery, OHCA) Compliance on ThoraxBelt after discharge An X-ray examination at an outpatient clinic

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rib Fractures, Pain, Thorax; Fracture
Keywords
Rib fractures, pain control, Posthorax Thoraxbelt

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care ProviderOutcomes Assessor
Masking Description
The surgeon will not know the patients' group before or during the surgery. The outcome assessor will not know the group during the whole research.
Allocation
Randomized
Enrollment
112 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
ThoraxBelt (Inpatients)
Arm Type
Experimental
Arm Description
Received ThoraxBelt after the surgery in addition to oral analgesics. Standard care for pain management will be the same as the Standard Care Arm (Inpatients).
Arm Title
Standard Care (Inpatients)
Arm Type
No Intervention
Arm Description
Standard Care with IV PCA and on-request oral painkiller.
Arm Title
ThoraxBelt (Outpatients)
Arm Type
Experimental
Arm Description
Received ThoraxBelt at the emergency room in addition to oral analgesics. Standard care for pain management will be the same as the Standard Care Arm (Outpatients).
Arm Title
Standard Care (Outpatients)
Arm Type
No Intervention
Arm Description
Standard Care and on-request oral painkiller.
Intervention Type
Device
Intervention Name(s)
Posthorax Thoraxbelt
Intervention Description
The patients will be assisted to put on the ThoraxBelt after surgery or at the emergency room by our research members and will be asked to keep it on except for showering through the whole study period.
Primary Outcome Measure Information:
Title
Inpatients: Visual analog scale (VAS)
Description
A pain score will be assessed to each patient after the total amount of visual analog scale. The minimum is 0 and the maximum is 10, from the least pain to the highest pain.
Time Frame
48 hours
Title
Outpatients: Visual analog scale (VAS)
Description
A pain score will be assessed to each patient after the total amount of visual analog scale. The minimum is 0 and the maximum is 10, from the l
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Inpatients: IV PCA dose
Description
the accumulated IV PCA drug dose
Time Frame
48 hours
Title
Inpatients: On-request oral painkiller dose
Description
the accumulated oral painkiller dose
Time Frame
48 hours
Title
Inpatients: Complication during the hospital stay
Description
Any complications whether related to ThoraxBelt or not
Time Frame
48 hours
Title
Inpatients: Length of hospital stay
Description
the amount of days in hospital stay
Time Frame
1 month
Title
Inpatients: VAS before discharge
Description
Visual analog scale before discharge
Time Frame
3 months
Title
Inpatients: The amount of unanticipated events
Description
send to the ICU admission, a second surgery or death
Time Frame
3 months
Title
Inpatients: VAS in outpatient clinic follow-up
Description
VAS during the 1-week, 1-month and 3-month outpatient clinic visit after the surgery
Time Frame
3 months
Title
Inpatients/Outpatients: X-ray examination
Description
An X-ray examination at an outpatient clinic
Time Frame
3 months
Title
Inpatients/Outpatients: Compliance on ThoraxBelt after discharge
Description
How long is the ThroaxBelt removed except during the bath within the whole day. The unit is hour.
Time Frame
3 months
Title
Outpatients: Complication during the follow-up period
Description
Any complications whether related to ThoraxBelt or not
Time Frame
6 months
Title
Outpatients: The amount of unanticipated events
Description
send to the ward admission, ICU admission, a surgery or OHCA
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The adult patients with rib fractures (inpatients/outpatients) The patients will be assessed to the further admission (inpatients) The patients will be assessed to be at follow-up clinic visit (outpatients) Exclusion Criteria: The accident of rib fractures has been occurred over 24 hours. (inpatients/outpatients) Refuse to be arranged to the admission (inpatients) Refuse to receive the CT scan (inpatients/outpatients) Chest wall infection or other diseases (inpatients/outpatients) Chest wall infected by rumors (inpatients/outpatients) Pregnancy (inpatients/outpatients) Further complications arise (inpatients/outpatients) Known allergy to ThoraxBelt (inpatients/outpatients)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Cheng-Yi Fan, M.D.
Phone
+886911438312
Email
chengyi.md@gmail.com
Facility Information:
Facility Name
National Taiwan University Hospital Hsin-Chu Branch
City
Hsinchu
ZIP/Postal Code
300
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Cheng-Yi Fan, MD
Phone
0911438312
Email
kpfzboekbof@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Currently, we have no plan on sharing the IPD.

Learn more about this trial

The Pain Control in Rib Fracture With Non-invasive Stabilization (RCT)

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