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Comparison between Platelet Rich Plasma(PRP) and corticosteroid in the treatment of knee osteoarthritis

The effects of intraarticular injection of Platelet Rich Plasma(PRP) and corticosteroid on knee osteoarthritis: a randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013041413012N1
Enrollment
40
Registered
2013-06-09
Start date
2013-03-10
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Gonarthrosis [arthrosis of knee]. Primary gonarthrosis, bilateral

Interventions

first group: Injection of 5 cc PRP (tubex, super PRP tube system) in the knee intraarticularly.
second group: injection of 40 mg corticosteroid (Depomedrol) in the knee intraarticularly.
Intervention 1: first group: Injection of 5 cc PRP (tubex, super PRP tube system) in the knee intraarticularly. Intervention 2: second group: injection of 40 mg corticosteroid (Depomedrol) in the knee
Treatment - Drugs

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion: knee osteoarthritis; VAS more than 60; use of at least two other methods of treatment previously. Exclusion: breast feeding; pregnancy; RA; severe cardiac disease; immunosuppresion; warfarin intake; coagulopathies; take NSAID or ASA during 5 days ago; radiculopathy; knee surgery during 3 months ago; active infection or malignancy; substance abuse; poor controlled diabetes mellitus; any knee injection during 6 months ago; doing physiotherapy or acupuncture during 6 months after injection

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain severity. Timepoint: before injection, 3 weeks, 2 and 6 months after injection. Method of measurement: VAS.;Time of 20 meters traverse. Timepoint: before injection, 3 weeks, 2 and 6 months after injection. Method of measurement: 20 meteres walk test.;Pain, symptomes and function of patient. Timepoint: before injection, 2 and 6 months after injection. Method of measurement: KOOS questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Bijan Forogh

Tehran University of Medical Sciences

bijanfr@gmail.com+98 21 8214 1229

Outcome results

None listed

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