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Evaluate Safety & Efficacy of Condroflex in Subjects With OA — ZD20108  

Osteoarthritis Clinical Trial

Official title:
Phase 3 Study, to Evaluate Safety & Efficacy of the Association Condroflex + Therapeutic Exercises Compared to Placebo + Therapeutic Exercises, in Subjects With Knee OA

Clinical Trial Summary

Primary Objective: To compare, after 12 weeks of double-blind treatment, the evolution of the improvement of pain (at rest and during / after exercise) in the questionnaire WOMAC (Western Ontario and McMaster Universities Arthritis Index), achieved with Condroflex ® oral administration(sulfate glucosamine + chondroitin sulfate sodium) in association with therapeutic exercises, compared to placebo in association with therapeutic exercises in individuals with knee OA and not exposed to prior treatment with the products under investigation.

Clinical Trial Description

To have osteoarthritis degree 2 or 3 / To be capable to consent ;

Study Design

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

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00838487
Study type Interventional
Source Zodiac Produtos Farmaceuticos S.A.
Contact Suely Roizenblatt
Phone 55 11 5908-7081
Email suelyroi@gmail.com
Status Recruiting
Phase Phase 3
Start date March 2009
Completion date March 2010
View Details
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