Skip to content

Study to Comapre the benefits and risk of Diacerein and Glucosamine in patients with Osteoarthritis.

Efficacy and safety of Diacerein versus Glucosamine in patients with osteoarthritis of the knee:A prospective comparative study.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2019/01/017336
Enrollment
50
Registered
2019-01-31
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M171- Unilateral primary osteoarthritisof knee

Interventions

Control Intervention1: Diacerein Versus Glucosamine: Patients with newly diagnosed osteoarthritis of the knee who are to be started on Diacerein or Glucosamine will be selected for the study. Those P

Sponsors

Dr Sruthi N
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Patient between 50 to 65 years with knee osteoarthritis(satisfying American college of rheumatology clinical criteria and Kellgren â?? Lawrence grade 2 or 3) 2) Patient who are willing to participate and signed in written informed consent

Exclusion criteria

Exclusion criteria: 1) Pregnancy and lactation. 2) Patients with Gastro intestinal, renal and liver diseases and diabetes. 3) Patients with acute exacerbation of OA at the time of enrolment. 4) Secondary OA and other rheumatologic diseases. 5) Patient who had undergone knee surgeries. 6) Patients who are on physical modalities from the department and patients with history of intra articular injections.

Design outcomes

Primary

MeasureTime frame
Efficacy will be evaluated primarily by the decrease in WOMAC and VAS score. Safety will be evaluated by assessing for any adverse drug reactions and causality. The number of Paracetamol tablets used and the swelling and tenderness of knee joint will also be evaluated as secondary outcomes.Timepoint: Duration of follow-up: 1 year. Follow up visits will be scheduled on 1 month, 2month, 3month and 4month.

Secondary

MeasureTime frame
The number of Paracetamol tablets used and the swelling and tenderness of knee joint will also be evaluated as secondary outcomes.Timepoint: Follow up visits will be scheduled on 1 month, 2month, 3month and 4month.

Countries

India

Contacts

Public ContactDr Sruthi N

Government Medical College Kozhikode

anuradha.m1@gmail.com9947624683

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026