Clinical Trials Directory

Trials / Completed

CompletedNCT00860873

Effectiveness of Glucosamine + Chondroitin in Osteoarthrosis

Randomized Study of Two Dosage Forms (Oral Powder and Capsule) of "Chondroitin + Glucosamine Sulfate" Produced by the Laboratory EMS When Compared to the Product Condroflex (Oral Powder and Capsules) Produced by Laboratory Zodiac in the Treatment of Osteoarthrosis.

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
280 (actual)
Sponsor
Azidus Brasil · Industry
Sex
All
Age
30 Years – 80 Years
Healthy volunteers
Accepted

Summary

This study objective is to check the non-inferiority of the 2 formulations produced by EMS when compared with the same substances and pharmaceuticals forms of the product Condroflex (Zodiac), by promoting the relief of osteoarthrosis symptoms such as pain, stiffness and functional capacity that will be periodically measured by using the "Visual Analog Scale" of pain (VAS) and the questionnaire of Lequesne.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTEMS Chondroitin Sulfate + Glucosamine Sulfate (Oral powder)Chondroitin Sulfate 1200mg Glucosamine Sulfate 1500mg
DIETARY_SUPPLEMENTEMS Chondroitin Sulfate 1200mg + Glucosamine Sulfate 1500mg (hard capsules)Chondroitin Sulfate 1200mg Glucosamine Sulfate 1500mg
DIETARY_SUPPLEMENTZodiac: Chondroitin Sulfate 1200mg + Glucosamine Sulfate 1500mg (Oral powder)Chondroitin Sulfate 1200mg + Glucosamine Sulfate 1500mg
DIETARY_SUPPLEMENTZodiac Chondroitin Sulfate 1200mg + Glucosamine Sulfate 1500mg (hard capsules)Chondroitin Sulfate 1200mg + Glucosamine Sulfate 1500mg

Timeline

Start date
2009-10-01
Primary completion
2009-11-01
Completion
2010-11-01
First posted
2009-03-12
Last updated
2013-02-25

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT00860873. Inclusion in this directory is not an endorsement.