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NOT YET RECRUITING
NCT07689162
PHASE2

Liposomal Bupivacaine vs Standard Bupivacaine for Post-Rhinoplasty Analgesia

Sponsor: Washington University School of Medicine

View on ClinicalTrials.gov

Summary

The purpose of this study is to find out which pain medication is more effective in reducing pain after nose surgery (rhinoplasty). The investigators are looking to find the best treatment to reduce discomfort and improve the healing process for patients having nose surgery.

Official title: Liposomal Bupivacaine vs Standard Bupivacaine for Post-Rhinoplasty Analgesia: A Randomized Clinical Trial

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

45

Start Date

2026-07

Completion Date

2027-07

Last Updated

2026-07-10

Healthy Volunteers

No

Interventions

DRUG

Standard Bupivacaine

Volume: 4 mL of 0.75% bupivacaine hydrochloride

DRUG

Liposomal Bupivacaine

Volume: 1.5 mL of 0.75% bupivacaine hydrochloride and 2.5 mL of liposomal bupivacaine

Locations (1)

Washington University

St Louis, Missouri, United States