CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 158 enrolled
Drug / intervention
CS+SG +1 moredrug
Likely dose
Not stated in 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/NCT01893905
NCT01893905Phase 3Completed

Phase III Clinical Trial to Evaluate the Efficacy and Safety of Chondroitin Sulfate and Glucosamine Sulfate in Combination Versus Placebo in Patients With Osteoarthritis of the Knee

Tedec-Meiji Farma, S.A.·interventional·Posted Jul 9, 2013·Updated Aug 4, 2017

In Brief

A Phase 3 clinical trial evaluating CS+SG and Placebo for Knee Osteoarthritis. Completed, enrolled 158 participants across 1 site.

Detailed Summary

The main objective is to assess the efficacy of a new formulation containing chondroitin sulfate and glucosamine sulfate (CS+GS) compared with placebo in patients with primary osteoarthritis of the knee.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesSpain
Collaborators--

Timeline

Phase 3CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedJul 9, 2013
Enrollment StartJun 1, 2013
Primary CompletionAug 1, 2014
TodayJul 2, 2026
Enrollment to primary: 1.2 yearsPosted 13.0 years ago

Interventions

CS+SGdrug

Chondroitin sulfate+glucosamine sulfate orally administered once a day for 24 weeks.

Placebodrug

Placebo of chondroitin sulfate+glucosamine sulfate orally administered once a day for 24 weeks.