CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 200 enrolled
Drug / intervention
clindamycin +1 moredrug
Likely dose
clindamycin 20mg/kgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00352612
NCT00352612Phase 4Completed

Comparison of Cephalexin Versus Clindamycin in the Empiric, Outpatient Treatment of Suspected Staphylococcal Cutaneous Infections in the Era of Community-associated Methicillin-resistant Staphylococcus Aureus (CA-MRSA)

Aaron Chen·interventional·Posted Jul 14, 2006·Updated May 13, 2013

In Brief

A Phase 4 clinical trial evaluating clindamycin and cephalexin for Staphylococcal Infection and 3 related conditions. Completed, enrolled 200 participants across 1 site.

Detailed Summary

The purpose of this study is to help define the role of antibiotics in the treatment of pediatric skin infections caused by community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA). The investigators hypothesize that treatment with cephalexin, a penicillin-like antibiotic to which CA-MRSA would be expected to be resistant, does not result in poorer outcomes than treatment with clindamycin, an antibiotic to which CA-MRSA is most often susceptible.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 4CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJul 14, 2006
Enrollment StartSep 1, 2006
Primary CompletionMay 1, 2009
Study CompletionAug 1, 2009
TodayJul 2, 2026
Enrollment to primary: 2.7 yearsPosted 20.0 years ago

Interventions

clindamycindrug

clindamycin suspension or tablets, 20mg/kg/day, given by mouth, divided TID, for 7 days

cephalexindrug

cephalexin suspension or tablets, 40mg/kg/day, given by mouth, divided TID, for 7 days