Clinical Trial

Antibiotic Prophylaxis in Rhinoplasty

Enrolling by Invitation Phase 3
View on ClinicalTrials.gov →
Summary
This study compares the efficacy of a single intra-operative (intravenous) dose of "cephalexin" (first generation cephalosporin) or "clindamycin" (lincosamides), alone versus both intra-operative (intravenous) dose of "cephalexin" (first generation cephalosporin) or "clindamycin" (lincosamides) and postoperative oral dose of "cephalexin" or "clindamycin" use in nasal surgery.
Protocol Amendment History 8 amendments
This ClinicalTrials.gov record has been amended 8 times since 2019-12-09; most recent amendment 2026-04-21.
Status change: Not Yet Recruiting → Enrolling by Invitation 2020-07-09
Trial Details
NCT Number NCT04194216
Lead Sponsor Stanford University
Collaborators: Washington University School of Medicine, Vanderbilt University School of Medicine, University of Washington, Duke University, Harvard University, University of Kansas Medical Center, University of Cincinnati, Loma Linda University
Conditions Nasal Obstruction, Nasal Surgical Procedures
Enrollment 864 participants
Start Date 2020-05-20
Primary Completion 2026-12-20 (estimated)
Study Completion 2027-04-20 (estimated)
Updated on ClinicalTrials.gov 2026-04-24