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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05321836
Other study ID # 333
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 26, 2021
Est. completion date March 25, 2022

Study information

Verified date April 2022
Source Neuro Counsel Hospital, Pakistan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

to see the effect of glucosamine chondratin sulfate with and without physiotherapy in knee osteoarthritis


Description:

it is a randomized control trail to evaluate the effectiveness of glucosamine chondratin sulfate alone and in combination with physiotherapy on knee osteoarthritis


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date March 25, 2022
Est. primary completion date March 25, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 50 Years and older
Eligibility Inclusion Criteria: - age > 50 years with radiographic evidence of mild to moderate knee OA (Kellgren Lawrence grade II & III 20) who met the ACR clinical 21, - radiographic classification criteria or confirmation of mild to moderate radiographic evidence of knee OA from a personal physician - not currently participating in another intervention study Exclusion Criteria: - dementia (Mini-Mental State Examination [MMSE]< 24) - active cancer other than skin cancer - anemia (participants with an hematocrit (HCT)< 32 (or a hemoglobin below10) were excluded due to possible inability to adequately exercise or the increased potential for increased risk for serious adverse cardiovascular events) - severe renal insufficiency (serum creat> 2) - hepatic disease

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Glucosamine Chondroitin
control group
Combination Product:
glucosamine chondritin & Physiotherapy
experimental group

Locations

Country Name City State
Pakistan Muhammad Umar Rawalpindi Punjab

Sponsors (1)

Lead Sponsor Collaborator
Muhammad salman, PT

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary WOMAC higher score means worst patient condition and lower score means better 6 months
Secondary SF-36 higher score means better patient condition and lower score means worst 6 months
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