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A Multicentre, Randomized as a Double Blind Study, Triple Placebo, Comparative of the Efficacy and Safety of an Association Secnidazol-Ciprofloxacin Compared With Amoxicillin-Clavulanic Acid for the Treatment of Uncomplicated Episode of Diverticular Sigmo

2014-07-23 21:08:54 | BioPortfolio

Summary

The primary outcome measure is to compare efficacy of an association of Secnidazol(2g)-Ciprofloxacin(1g) (during 3 days) versus 3g of Amoxicillin-Clavulanic Acid during 10 days for the Treatment of Uncomplicated Episode of Diverticular Sigmoïditis Among Adults in clinical and biological cure.

The cure rate will be evaluated at the second visit (14 days after the inclusion visit).

Study Design

Allocation: Randomized, Control: Active Control, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Conditions

Diverticular Sigmoïditis

Intervention

Secnidazole, ciprofloxacine, Amoxicillin-Clavulanic Acid

Location

QuantaMedical
Rueil Malmaison
France
92507

Status

Recruiting

Source

Laboratoires IPRAD

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-07-23T21:08:54-0400

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