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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04980105
Other study ID # UOW/MS102
Secondary ID
Status Active, not recruiting
Phase Phase 3
First received
Last updated
Start date March 2, 2020
Est. completion date October 1, 2021

Study information

Verified date July 2021
Source University of Wasit
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To assess if there are any differences among platelet-rich plasma, hyaluronic acid, and corticosteroid knee intra-articular injection regarding function and pain.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 150
Est. completion date October 1, 2021
Est. primary completion date September 1, 2021
Accepts healthy volunteers No
Gender All
Age group 35 Years to 65 Years
Eligibility Inclusion Criteria: - Patient aged 35-65 years old - Patient with knee pain that had been continuing for at least 12 months with no relief using anti-in?ammatory medications and that deteriorated with weight-bearing - Knee osteoarthritis that classified as mild-moderate or moderate-severe (Kellgren-Lawrence Grade 2, 3, or 4) Exclusion Criteria: - Age > 65 years - The recent history of knee trauma - Autoimmune rheumatic diseases - Accompanying severe hip OA - Thrombocytopenia or other blood diseases - Immunosuppressive or anticoagulant treatment - The invasive procedure applied to the knee - Intra-articular steroid injection to the knee within the previous 12 months - Previous joint infection - Uncontrolled systemic diseases such as diabetes or hypertension, and cancer - Excessive varus/valgus knee deformity

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
Platelet-rich plasma
Two intra-articular injections of autologous platelets-rich plasma (PRP) in two weeks intervals between the first and the second injection.
Drug:
Hyaluronic acid
Two intraarticular injections of hyaluronic acid (60 mg) in two weeks intervals between the first and the second injection
Methylprednisolone acetate injectable suspension (DEPO-MEDROL®)
Single methylprednisolone acetate intraarticular injection (DEPO-MEDROL® pfizer 80 mg) mixed with 3cc of (xylocaine 2% concentration)

Locations

Country Name City State
Iraq University of Wasit Wasit

Sponsors (1)

Lead Sponsor Collaborator
University of Wasit

Country where clinical trial is conducted

Iraq, 

Outcome

Type Measure Description Time frame Safety issue
Primary Timed Up and Go test (TUG) The Timed Up and Go test (TUG) is a simple test used to assess a person's mobility and requires both static and dynamic balance. It uses the time that a person takes to rise from a chair, walk three meters, turn around 180 degrees, walk back to the chair, and sit down while turning 180 degrees 18th months
Primary Visual Analogue Scale (VAS) The VAS uses a straight 10 centimeter line with one end being 'no pain' and on the other end the 'worst imaginable pain'. The patient chooses a spot on the line then places a perpendicular line to indicate their pain level 18th months
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