Status:
TERMINATED
Evaluating Postoperative Non-Opioid Pain Management Utilizing Local Anesthetics Coupled With Modulated Coagulation
Lead Sponsor:
NYU Langone Health
Conditions:
Opioid Pain Medication
Eligibility:
All Genders
18-99 years
Phase:
PHASE4
Brief Summary
This study is a prospective randomized trial examining the effect of topically combined antifibrinolytics (Tranexamic acid) with local anesthetics in all electively created surgical wound beds in hand...
Detailed Description
The aim of the study is to provide long term pain relief and decrease the use of postoperative narcotics. All treatments are applied topically to the surgical bed prior to closure of the skin. Each of...
Eligibility Criteria
Inclusion
- Age 18 or older
- Any patient undergoing elective hand surgery
Exclusion
- Any patient with a traumatic open wound (only surgically created wounds will be included)
- History of chronic pain
- History of narcotic addiction
- History of recreational drug dependency
- History of psychiatric pathology
- Allergy to local anesthetics, recombinant human thrombin or tranexamic acid
- Any patient receiving a supra/infraclavicular block for anesthesia
Key Trial Info
Start Date :
March 24 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 10 2023
Estimated Enrollment :
46 Patients enrolled
Trial Details
Trial ID
NCT04814433
Start Date
March 24 2021
End Date
July 10 2023
Last Update
June 26 2024
Active Locations (1)
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1
NYU Langone Health
New York, New York, United States, 10016