Status:
COMPLETED
Efficacy of Hematoma Block on Postoperative Pain After Femoral Intramedullary Rodding: A Randomized Trial
Lead Sponsor:
University of Cincinnati
Conditions:
Femur Fracture
Eligibility:
All Genders
18+ years
Phase:
PHASE4
Brief Summary
The purpose of this study is to evaluate the efficacy of an intra-operative, post-fixation fracture hematoma block compared to saline control on postoperative pain control in patients with acute femor...
Detailed Description
This blinded, randomized control trial is being performed at the University of Cincinnati Medical Center. Patients will be randomly assigned to one of two treatment groups: Group One will be comprise...
Eligibility Criteria
Inclusion
- Trauma patient at the University of Cincinnati Medical Center
- Skeletally mature patients
- Have an isolated, closed, acute traumatic femoral shaft fracture to be treated with a closed reduction and reamed intramedullary rod fixation
Exclusion
- Unable to provide informed consent
- Member of a vulnerable patient population
- Have additional injuries
- Have a history of prior existing narcotic use or chronic pain management issues on presentation
Key Trial Info
Start Date :
August 17 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 7 2023
Estimated Enrollment :
88 Patients enrolled
Trial Details
Trial ID
NCT04860856
Start Date
August 17 2019
End Date
February 7 2023
Last Update
February 16 2023
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
University of Cincinnati College of Medicine
Cincinnati, Ohio, United States, 45267