check_circleStudy Completed

Bacterial Infection

Comparison of the efficacy and safety of ciprofloxacin with erythromycin in children with cholera.

Trial purpose

Please see attached Study Results Summary below

Key Participants Requirements

Sex

N/A

Age

2 - 10 Years
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Trial summary

Enrollment Goal
180
Trial Dates
May 2001 - July 2002
Phase
Phase 3
Could I Receive a placebo
N/A
Products
Cipro (Ciprofloxacin, BAYQ3939)
Accepts Healthy Volunteer
N/A

Trial design

An open, randomized clinical study comparing the efficacy and safety of a single dose of ciprofloxacin with erythromycin administered 6-hourly for 3 days in children with cholera
Trial Type
Interventional
Intervention Type
N/A
Trial Purpose
N/A
Allocation
N/A
Blinding
N/A
Assignment
N/A
Trial Arms
N/A