TerminatedPhase 4

A Study of Loco-Regional Liposomal Bupivacaine Injection

Stopped: Lack of funds

United States3 participantsStarted 2023-09-26

Plain-language summary

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.

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: \- Those who present for elective lower extremity revascularization. Exclusion Criteria: * Non-English speaking. * Chronic pain. * On opioids greater than 1 weeks. * Allergy to local anesthetics. * Use of spinal or epidural for surgery. * Lack of patient cooperation. * Contraindication to regional anesthesia. * Vulnerable individuals. * Urgent/emergent surgeries * Known to be pregnant or able to become pregnant

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Postoperative Use of Narcotics at 12 Hours

Timeframe: 12 hours after injection

Postoperative Use of Narcotics at 24 Hours

Timeframe: 24 hours after injection

Postoperative Use of Narcotics at 48 Hours

Timeframe: 48 hours after injection

Postoperative Use of Narcotics at 72 Hours

Timeframe: 72 hours after injection

Postoperative Use of Narcotics at 30 Days

Timeframe: 30 days after injection

Trial details

NCT IDNCT05992896

SponsorMayo Clinic

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-05-15

Results submitted2026-04-06

View on ClinicalTrials.gov More Peripheral Arterial Disease trials