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PVB vs Ketamine/Lidocaine in Rib Fracture Patients

Primary Purpose

Rib Fractures, Rib Trauma, Rib Fracture Multiple

Status
Recruiting
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
lidocaine, ketamine intravenous infusion
paravertebral block with ropivicaine
Sponsored by
George Washington University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Rib Fractures

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • age 18-80 with rib fracture requiring hospitalization
  • Failure of standard pain regimen as determined by RR > 20, TV < or equal to 50% predicted, NPS > or equal to 5, Poor cough

Exclusion Criteria:

  • age less than 18 years
  • greater than 80 years
  • GCS less than or equal to 13
  • intubated at admission
  • prior or anticipated exploratory laparotomy during this admission
  • prior or expected thoracotomy during this admission
  • prior or expected emergent craniotomy during this admission
  • spinal cord injury
  • pelvic injury that has required or will require operative intervention
  • inability to accomplish activities of daily living independently
  • pregnancy
  • incarceration

Sites / Locations

  • The George Washington University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

lidocaine/ ketamine infusion

paravertebral block with ropivacaine

Arm Description

Lidocaine/ ketamine infusion will be monitored and titrated as necessary by Anesthesiologist led Acute Pain Service.

Paravertebral block catheter will be placed by Anesthesiology led Acute Pain Service. Once the catheter is inserted, a ropivacaine bolus and infused with ropivacaine, monitored and titrated as necessary by Anesthesiologist led Acute Pain Service.

Outcomes

Primary Outcome Measures

Numeric Pain Score (NPS)
Numeric pain score is a scale of 1- 10 to ascertain patient's subjective pain severity. Patients will be asked their NPS daily.
Oral Morphine Equivalence (OME)
Oral morphine equivalence is used to standardized the amount of opioid patient is using regardless the type of opioid that the patient is prescribed.

Secondary Outcome Measures

Hospital Length of Stay (LOS)
The hospital length of stay will be captured after patient is discharged from the hospital.
ICU Length of Stay (ICU LOS)
The ICU length of stay will be captured after patient is discharged from the hospital.
incidence of pneumonia
The diagnosis of pneumonia is captured when it is diagnosed by the primary team taking care of the patient.
ventilator days
We will obtain the number of days patient is on the ventilator
disposition upon discharge
Patient's disposition after discharge will be recorded. Disposition of patient will be recorded as home, long term acute facility, skilled nursing facility or acute rehab
in-hospital mortality
Patient's death will be recorded if it happen before discharge

Full Information

First Posted
May 26, 2020
Last Updated
January 3, 2023
Sponsor
George Washington University
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1. Study Identification

Unique Protocol Identification Number
NCT04413799
Brief Title
PVB vs Ketamine/Lidocaine in Rib Fracture Patients
Official Title
Paravertebral Block Versus Simultaneous Ketamine and Lidocaine Infusions for Pain Management in Rib Fracture Patients
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2020 (Actual)
Primary Completion Date
December 2024 (Anticipated)
Study Completion Date
May 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
George Washington University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Rib fractures are a common admission to the trauma service. The mainstay of treatment is pain control to improve respiratory effort in order to offset the risk of pneumonia and mechanical ventilation. In addition to standard pain control modalities, the investigator's institution utilizes paravertebral blocks as well as lidocaine and ketamine infusions for pain control. The current standard of care for pain control is to begin with acetaminophen, ibuprofen or celecoxib and opioids with the addition of paravertebral blocks as needed. In certain situations, a paravertebral block is contraindicated, and pain control is relegated to lidocaine and ketamine infusion. The use of lidocaine infusion alone and ketamine infusion alone for pain control has been studied and has been shown to be safe. However, concurrent use of these two medications to control rib fracture pain is relatively new and the efficacy compared to paravertebral block is not known. The goal of the study is to show non-inferiority of simultaneous lidocaine and ketamine infusions versus paravertebral blocks.
Detailed Description
Traumatic rib fractures are a common pathology in the trauma population. It is estimated that 10% of all trauma patients have rib fractures. The mainstay of treatment of rib fracture is pain control to allow for good pulmonary hygiene and function. When pain is not controlled, patients have a higher chance of developing pneumonia, which can lead to respiratory failure needing mechanical ventilation, eventually increasing patients' morbidity and mortality. These sequelae are most common in the elderly population. Multiple studies has shown that elderly patients with rib fractures have worse outcomes compared to younger patients with the same fracture pattern. Pain control for acute rib fracture is achieved using multimodal analgesia to reduce the usage of opioids. Multimodal analgesia means using 2 or more drugs that act by different mechanism to provide pain control. The benefit of multimodal strategy is twofold; decrease the use of opioids and the associated side effects (eg. depressed respiratory drive, delirium, alteration of mental status) and better pain control. However, even with multimodal analgesia, pain control for acute traumatic rib fractures can be challenging. There are currently no validated management guidelines for traumatic rib fracture pain control and the approach varies by organization. At the investigator's institution, the investigators use a scheduled regimen of acetaminophen and NSAIDs, along with opioid medication as needed for pain. If this regimen is insufficient, other adjuncts such as paravertebral blocks (PVBs) and intravenous ketamine and lidocaine infusions are utilized. There are currently limited data on the combined use of ketamine and lidocaine infusions for traumatic rib fractures and it is unclear if the combination is non-inferior to PVBs in this patient population. Continuous PVB infusion is a well-documented approach for pain control in traumatic rib fractures. But, there are occasionally prohibitive situations that contraindicate PVBs, such as vertebral fractures. Ketamine and lidocaine infusions are an attractive alternative in these situations, but the data regarding efficacy are lacking. Low dose ketamine infusion is a new addition to the pain control algorithm for trauma patients. Given that this is a novel approach, studies evaluating efficacy are sparse. There have been two randomized controlled trials utilizing low dose ketamine in trauma patients and elderly patients with rib fractures. Both were unable to show a decrease in opioid use; however, the authors were able to show a decrease in pain scores in patients with injury severity score (ISS) >15 in both studies. Another study of ketamine infusion in traumatic rib fracture patients admitted to the ICU showed an improvement in numeric pain scores (NPS) and decreased opioids requirements but, as in the previous studies, the ISS of these patients was very high (40) in both the ketamine and non-ketamine groups making generalization to the overall trauma population difficult. Lidocaine has also been extensively studied as a local anesthetic and more recently has become popular as an infusion for systemic pain control. A recent review article compared 16 randomized control trials of lidocaine infusion on postoperative patients and showed that patients undergoing abdominal surgery had significant decreases in postoperative opioid consumption and improved pain scores. There has been some research into lidocaine infusions in burn patients showing that it can decrease opioid usage by 25%, but the cohort was small and there was no difference in reported pain scores. These data are intriguing but the applicability to trauma patients is questionable. Unfortunately, there has been no study to assess lidocaine infusions in patients with traumatic rib fractures. The investigators believe that there is a role for simultaneous lidocaine and ketamine infusions in traumatic rib fracture patients that may provide better pain control than each one used as a single infusion. The investigators propose a prospective, randomized open label clinical trial evaluating continuous infusion of ropivacaine via PVBs against simultaneous ketamine and lidocaine infusions. The instigators hypothesize that simultaneous lidocaine and ketamine infusions is non inferior to PVBs in traumatic rib fracture patients. The results of this study could help guide pain control strategies in this patient population.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rib Fractures, Rib Trauma, Rib Fracture Multiple, Pain, Acute

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
170 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
lidocaine/ ketamine infusion
Arm Type
Active Comparator
Arm Description
Lidocaine/ ketamine infusion will be monitored and titrated as necessary by Anesthesiologist led Acute Pain Service.
Arm Title
paravertebral block with ropivacaine
Arm Type
Active Comparator
Arm Description
Paravertebral block catheter will be placed by Anesthesiology led Acute Pain Service. Once the catheter is inserted, a ropivacaine bolus and infused with ropivacaine, monitored and titrated as necessary by Anesthesiologist led Acute Pain Service.
Intervention Type
Combination Product
Intervention Name(s)
lidocaine, ketamine intravenous infusion
Intervention Description
Patients will be started with our standard analgesia regiment which is standing oral acetaminophen 1000mg every 8 hours, ibuprofen 600mg every 6 hours or celecoxib 200mg every 12 hours, and narcotics as needed. All patients who failed the standard analgesia regimen will be approached for the study. Failure of standard analgesia regimen will be determined by respirations >20 minute, tidal volume ≤50% of predicted, numeric pain score ≥ 5, and a poor cough as determined by the trauma team. Once the consent is obtained, the patients will be randomized to either PVB (control) or lidocaine/ketamine (study) groups. If the patient is randomized to lidocaine/ketamine group, the anesthesiologist led Acute Pain Service (APS) will prescribe lidocaine/ ketamine infusion, which will be monitored and titrated as necessary by APS. Standard analgesia will be continued on both study groups
Intervention Type
Drug
Intervention Name(s)
paravertebral block with ropivicaine
Intervention Description
Patients will be started with our standard analgesia regiment which is standing oral acetaminophen 1000mg every 8 hours, ibuprofen 600mg every 6 hours or celecoxib 200mg every 12 hours, and narcotics as needed. All patients who failed the standard analgesia regimen will be approached for the study. Failure of standard analgesia regimen will be determined by respirations >20 minute, tidal volume ≤50% of predicted, numeric pain score ≥ 5, and a poor cough as determined by the trauma team. Once the consent is obtained, the patients will be randomized to either PVB (control) or lidocaine/ketamine (study) groups. If the patient is randomized to PVB, the anesthesiologist led Acute Pain Service (APS) will place a paravertebral block catheter. Ropivacaine infusion will be started, monitored and titrated as necessary by APS. Standard analgesia will be continued on both study groups
Primary Outcome Measure Information:
Title
Numeric Pain Score (NPS)
Description
Numeric pain score is a scale of 1- 10 to ascertain patient's subjective pain severity. Patients will be asked their NPS daily.
Time Frame
throughout patients' hospitalization time, an average of 1 week
Title
Oral Morphine Equivalence (OME)
Description
Oral morphine equivalence is used to standardized the amount of opioid patient is using regardless the type of opioid that the patient is prescribed.
Time Frame
throughout patients' hospitalization time, an average of 1 week
Secondary Outcome Measure Information:
Title
Hospital Length of Stay (LOS)
Description
The hospital length of stay will be captured after patient is discharged from the hospital.
Time Frame
captured after patient is discharged, an average of 1 week
Title
ICU Length of Stay (ICU LOS)
Description
The ICU length of stay will be captured after patient is discharged from the hospital.
Time Frame
captured after patient is discharged, an average of 1 week
Title
incidence of pneumonia
Description
The diagnosis of pneumonia is captured when it is diagnosed by the primary team taking care of the patient.
Time Frame
throughout patients' hospitalization time, an average of 1 week
Title
ventilator days
Description
We will obtain the number of days patient is on the ventilator
Time Frame
throughout patients' hospitalization time, an average of 1 week
Title
disposition upon discharge
Description
Patient's disposition after discharge will be recorded. Disposition of patient will be recorded as home, long term acute facility, skilled nursing facility or acute rehab
Time Frame
captured after patient is discharged, an average of 1 week
Title
in-hospital mortality
Description
Patient's death will be recorded if it happen before discharge
Time Frame
captured after patient is discharged, an average of 1 week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age 18-80 with rib fracture requiring hospitalization Failure of standard pain regimen as determined by RR > 20, TV < or equal to 50% predicted, NPS > or equal to 5, Poor cough Exclusion Criteria: age less than 18 years greater than 80 years GCS less than or equal to 13 intubated at admission prior or anticipated exploratory laparotomy during this admission prior or expected thoracotomy during this admission prior or expected emergent craniotomy during this admission spinal cord injury pelvic injury that has required or will require operative intervention inability to accomplish activities of daily living independently pregnancy incarceration
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Susan Kartiko, MD PhD
Phone
7136776219
Email
skartiko@mfa.gwu.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Tremaine Brock
Email
tbrock@mfa.gwu.edu
Facility Information:
Facility Name
The George Washington University Hospital
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20037
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Susan Kartiko, MD PhD
Phone
713-677-6219
Email
skartiko@mfa.gwu.edu
First Name & Middle Initial & Last Name & Degree
Paul Dangerfield, MD
Email
pdangerfield@mfa.gwu.edu

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
IPD will not be shared with other researchers.
Citations:
PubMed Identifier
7996614
Citation
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PVB vs Ketamine/Lidocaine in Rib Fracture Patients

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