Antibiotic Prophylaxis in Rhinoplasty

Status Enrolling by invitation

Clinical Trial 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.

Clinical Trial Description

The study will consist of 2 treatment arms: Treatment arm A: Intra-operative single intravenous(iv) dose of "cephalexin" 2 g or "clindamycin" 900 mg. Treatment arm B: Intra-operative single intravenous(iv) dose of "cephalexin" 2 g or "clindamycin" 900 mg and postoperative oral dose of "cephalexin" 250mg every 4 hours or "clindamycin" 150mg every 6 hours, for a duration of three days. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04194216
Study type	Interventional
Source	Stanford University
Contact
Status	Enrolling by invitation
Phase	Phase 3
Start date	May 20, 2020
Completion date	April 20, 2025

View Details

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