Liposomal vs Standard Bupivacaine for Post-Rhinoplasty Pain
Official title: Liposomal Bupivacaine vs Standard Bupivacaine for Post-Rhinoplasty Analgesia: A Randomized Clinical Trial
Run by Washington University School of Medicine · NCT07689162 · Data updated 2026-11-12
This study tests whether liposomal bupivacaine provides better pain control after rhinoplasty than standard bupivacaine.
Quick facts
| Phase | Phase 2 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 45 (estimated) |
| Sponsor | Washington University School of Medicine Academic / other |
| Locations | 1 site (St Louis, Missouri) |
| Status | Recruiting |
| Started | August 1, 2026 |
| Main results expected | June 2027 |
| Study ends | July 2027 |
| Registry record updated | August 18, 2026 |
| Trial ID | NCT07689162 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (18+) undergoing open rhinoplasty (primary, revision, functional, or cosmetic) with any grafting type.
✕Probably not a fit
Patients with contraindications to local anesthetics or those with chronic pain requiring ongoing analgesics may not benefit from this intervention.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
In this Phase 2 interventional trial, adults undergoing open rhinoplasty are randomly assigned to receive either liposomal bupivacaine or standard bupivacaine as a nerve block during surgery. Pain levels are tracked for several days after the procedure, and safety and recovery are monitored. The goal is to determine which formulation more effectively reduces postoperative pain and supports smoother healing. The study is conducted at Washington University School of Medicine in St. Louis.
Why it matters
Potential benefit: If liposomal bupivacaine proves more effective, patients may experience less pain and faster recovery after rhinoplasty.
How similar studies have gone: Previous studies in other surgical settings have shown varying benefits of liposomal bupivacaine; results in rhinoplasty specifically are being evaluated in this trial.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult patients (≥18 years) undergoing open rhinoplasty of any indication or complexity (e.g., primary, revision, functional, or cosmetic), including autologous grafting of any type (e.g., septal or costal cartilage) or cadaveric grafting. Exclusion Criteria: * Chronic pain condition requiring ongoing or scheduled analgesic therapy, or any diagnosis associated with chronic pain (e.g., fibromyalgia, chronic headache/migraine, neuropathic pain, complex regional pain syndrome), long-term opioid use (≥3 months, any agent), allergy or contraindication to local anesthetics, acetaminophen, ibuprofen / NSAIDs, tramadol, ketamine, Medrol (methylprednisolone) dose pack * Concurrent non-nasal surgery planned
Where it's running
-
Washington University
St Louis, Missouri, United States Recruiting
Study contacts
- Principal investigator: Matthew Wu, MD — Washington University School of Medicine
- Study coordinator: Matthew Wu, MD
- Email: mjwu@wustl.edu
- Phone: 314-362-0524
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.