Osteoarthritis Clinical Trial
Official title:
Best Effect of Viscosupplementation With Hyaluronic Acid and Triamcinolone in Patients With Knee Osteoarthritis. Prospective Randomized Study Between Two Different Applications Regimens
| Verified date | September 2013 |
| Source | University of Sao Paulo General Hospital |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | Brazil: Ethics Committee |
| Study type | Interventional |
Viscosupplementation by intra-articular injection of hyaluronate products has recently gained popularity as a treatment modality of gonarthritis.There is not, however, a consensus on the best method.Our objective is to evaluate what is the best dosage of viscosupplementation with hyaluronic acid (OSTEONIL®) associated with 1 ml (20 mg) of triamcinolone hexacetonide. One hundred and four patients with knee osteoarthritis (KOA) were divides into 2 groups of 52 patients each to receive either a single application of 3 ampoules of OSTEONIL® + 1ml of Hexacetonide of triamcinolone or three applications of 1 ampoule of OSTEONIL®, one per week for three weeks + 1ml of Hexacetonide of triamcinolone only in the first injection. Primary endpoint was clinical results expressed by Visual Analogic Scale of pain (VAS), Western Ontario and Mcmaster Universities (WOMAC) and Lequesne questionaires at one, three, six and 12 months after the procedure
| Status | Completed |
| Enrollment | 104 |
| Est. completion date | April 2014 |
| Est. primary completion date | March 2014 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 40 Years and older |
| Eligibility |
Inclusion Criteria: - Met the American College of Rheumatology criteria for hip osteoarthritis - No knee intraarticular injections in the last 6 months Exclusion Criteria: - Severe reaction to the procedure |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| Brazil | Instituto de Ortopedia e Traumatologia HC-FMUSP | São Paulo | SP |
| Lead Sponsor | Collaborator |
|---|---|
| University of Sao Paulo General Hospital |
Brazil,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | WOMAC | Pain and function assessment with WOMAC questionaire | 6 months | No |
| Primary | VAS | Pain assessment with Visual Analogic Scale (VAS) | 6 months | No |
| Primary | LEQUESNE | Pain and function assessment with Lequesne questionaire | 6 months | No |
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