Evaluating Postoperative Non-Opioid Pain Management Utilizing Local Anesthetics Coupled With Modulated Coagulation
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- STATUS
- Recruiting
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- End date
- Mar 1, 2024
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- participants needed
- 40
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- sponsor
- NYU Langone Health
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 surgery to provide long term pain relief and decrease the use of postoperative narcotics.
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 the drugs used in this study are Food and Drug Administration (FDA) approved and routinely used for pain relief. However, the route of administration of the drugs and addition of tranexamic acid or aminocaproic acid is considered off-label (outside of the FDA-approved indications) and therefore investigational.
Details
| Condition | Opioid Pain Medication |
|---|---|
| Treatment | Tranexamic Acid, Aminocaproic acid, Aminocaproic acid, Recombinant Human Thrombin, Recombinant Human Thrombin, Lidocaine Hydrochloride with Epinephrine, Bupivacaine Hydrochloride with Epinephrine |
| Clinical Study Identifier | NCT04814433 |
| Sponsor | NYU Langone Health |
| Last Modified on | 24 March 2022 |
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