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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02178137
Other study ID # TIH-Ortho-001
Secondary ID
Status Completed
Phase Phase 4
First received June 27, 2014
Last updated February 28, 2018
Start date June 2014
Est. completion date October 2017

Study information

Verified date February 2018
Source Indus Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

There has been intensive search for a substance that can have disease-modifying activity for osteoarthritis. A number of medications have been reported to be of benefit on slowing progression of knee OA. This trial will be the first head to head comparison of these medications.

Patients aged between age 40 to 65 will be enrolled. Patients will be assessed clinically using two scoring systems, the WOMAC index for knee arthritis and the SF 36 for overall physical and mental health. The knee X rays will be assessed on Kellgren and Lawrence grading and will also be measured for joint space narrowing at follow up. The response to arthritis medications on slowing down cartilage loss will be measured biochemically with COMP levels.


Recruitment information / eligibility

Status Completed
Enrollment 322
Est. completion date October 2017
Est. primary completion date September 2017
Accepts healthy volunteers No
Gender All
Age group 40 Years to 65 Years
Eligibility Inclusion Criteria:

- Patients of either sex aged between 40 to 65 years with mild to moderate osteoarthritis of the knees.

- Patients should have history of knee pain for at least 6 months and on the majority of days during the preceding month

- Each joint will be scored separately so one patient with bilateral knee osteoarthritis will be counted as 2 knees.

- The osteoarthritis will be graded on basis of clinical score as well as seen on appropriately positioned x rays using the Kellgren and Lawrence grading. (Tibio femoral osteophytes of at least 1 mm, Kellgren Lawrence grading of 2 or 3)

- Patients with diabetes are sent to the diabetes clinic and are included once their HbA1c level becomes normal.

- Patients giving Informed consent

Exclusion Criteria:

- Patients with severe end stage tricompartmental osteoarthritis of the knees .

- Presence of uncontrolled systemic disease like chronic liver and renal disease

- Patients with diagnosis other than osteoarthritis, such as knee arthritis due to rheumatoid disease, gout, post traumatic arthritis

- Patients with history of surgery to any knee will have that knee excluded

- Pregnant or lactating mothers

- Patients with chronic anaemia

- Patients who get an injection in their affected knee

Study Design


Intervention

Drug:
Diacerien

Glucosamine/Chondroitin

Placebo


Locations

Country Name City State
Pakistan The Indus Hospital Karachi Sind

Sponsors (1)

Lead Sponsor Collaborator
Indus Hospital

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in WOMAC score at 24 months in comparison to baseline score Hypothesis:- At least one of the intervention drug will result in an improvement of at least 20 points on the WOMAC score at end of 2 years as compared to the placebo when compared to base line score baseline, 24 months
Primary Change to the SF-36 score at 24 months in comparison to baseline score Hypothesis: At least one of the intervention drugs will result in an improvement of at least 20 points at end of two years when assessed using the SF36 total score as compared to the standard therapy placebo when compared with baseline score 24 months
Primary Mean differences in blood serum COMP levels of study arms 24 months
Secondary Change in WOMAC score at 6 months in comparison to baseline score 6 months
Secondary Change in WOMAC score at 12 months in comparison to baseline score 12 months
Secondary Change in WOMAC score at 18 months in comparison to baseline score 18 months
Secondary Change to the SF-36 score at 6 months in comparison to baseline score 6 months
Secondary Change to the SF-36 score at 12 months in comparison to baseline score 12 months
Secondary Change to the SF-36 score at 18 months in comparison to baseline score 18 months