A Study of Loco-Regional Liposomal Bupivacaine Injection
- Disease/Condition
- Peripheral Arterial Disease
- Drug/Device/Intervention
- Bupivacaine liposome
- Study type
- Interventional
- Intervention type
- drug
- Primary sponsor
- Mayo Clinic
- Location
- Eau Claire, United States of America
- Phase
- Phase 4
- Start date
- Sep 26, 2023
- End date
- Feb 01, 2024
- Enrollment
- 20 participants
Postoperative use of narcotics at 12 hours,Postoperative use of narcotics at 24 hours,Postoperative use of narcotics at 48 hours,Postoperative use of narcotics at 72 hours,Postoperative use of narcotics at 30 days
The purpose of this research is to find out if using liposomal bupivacaine solution
 (bupivacaine liposome) injections during lower extremity revascularization surgery will lower
 the amount of narcotic drugs used during and following the procedure.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT05992896
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT05992896 through Pure Global AI's free database. This Phase 4 trial is sponsored by Mayo Clinic and is currently Recruiting. The study focuses on Peripheral Arterial Disease. Target enrollment is 20 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.