Overview
Clinical Efficacy of Glucosamine Plus Diacerein Versus Mono-therapy of Glucosamine
Status:
Completed
Completed
Trial end date:
2014-10-01
2014-10-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to compare pain scores, WOMAC total and subscores, actual and change of joint space width and the rate of gastrointestinal side effects at 4, 8, 12, and 24 weeks between dual-therapy of diacerein and glucosamine versus a mono-therapy of glucosamine in OA patientsPhase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Ramathibodi HospitalTreatments:
Diacetylrhein
Criteria
Adult patients age 50 years or older who have been diagnosed as primary or secondaryosteoarthritis of the knee base on clinical criteria of American College of Rheumatology
Inclusion Criteria:
- Clinical diagnosis of primary osteoarthritis
- Mild deformity Clinical (having no varus or valgus deformity, no crepitus) ? Physical
examination grade 0 assessed by stress test Radiographic assessment
(Kellgrane-lawrance type II-III), a minimum baseline medial tibiofemoral JSW of _2 mm.
- Willing to participate and provide written informed consent
Exclusion Criteria:
- Non-secondary osteoarthritis Rheumatoid arthritis, inflammatory arthritis (e.g. SLE,
Gout), post traumatic osteoarthritis, those who received intra-articular treatment of
the signal joint with any product (corticosteroids in the previous 2 months, or
glycosaminoglycans/hyaluronic acid in the previous 6 months) or had undergone joint
lavage andarthroscopic procedures in the previous 6 months.
- No contraindication of using diacerein and glucosamine
- Non-current or ex-users of oral SYSADOA (e.g., glucosamine sulphate, chondroitin
sulphate, diacerein, piascledine), anti-depressants, tranquillisers, antacids or
antibiotics known hypersensitivity to diacerein, to similar compounds, to the
excipients or to paracetamol