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Efficacy Study of Methenamine + Methylthioninium Chloride vs Phenazopyridine for the Symptomatic Control of Dysuria

Dysuria Clinical Trial

Official title:
Phase III, Prospective, Multicenter, Single-blind, Randomized, Superiority to Evaluate the Efficacy and Safety of Methenamine Association 250mg + Methylthioninium Chloride 20 mg Compared to Phenazopyridine 100 mg in Symptomatic Control of Dysuria

Clinical Trial Summary

The purpose of this study is to evaluate the efficacy of the combination of Methenamine + Methylthioninium chloride compared to phenazopyridine (comparator product) in the symptomatic relief of dysuria.

Clinical Trial Description

- Single blind, randomized, prospective study.

- Length of experience: 03 days to 07 days.

- 03 visits (days 1, 4 and 7).

- Evaluation of the efficacy and safety of the medication.

- Shall be assessed for adverse events. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01657448
Study type Interventional
Source EMS
Contact
Status Completed
Phase Phase 3
Start date June 27, 2016
Completion date December 22, 2017
View Details
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