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Comparison of PRP injection with or without high-power laser for knee osteoarthritis

Comparison of the short-term efficacy of intra-articular platelet-rich plasma injection alone versus intra-articular platelet-rich plasma injection combined with high-power laser therapy on pain and physical function in patients with grade 1-3 knee osteoarthritis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20260420069117N1
Enrollment
48
Registered
2026-05-20
Start date
2026-04-30
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Knee osteoarthritis (Knee OA) is a chronic degenerative joint disease characterized by progressive destruction of articular cartilage, synovial inflammation, and subchondral bone changes. It leads to persistent pain, stiffness, and functional disability. This study specifically includes patients with grade 1, 2, or 3 knee osteoarthritis based on radiographic criteria (Kellgren-Lawrence classification).. Osteoarthritis of knee, unspecified

Interventions

Intervention 1: Control group: Platelet-rich plasma (PRP) injection alone. Preparation method: 20 mL of venous blood is drawn with 3 mL of anticoagulant (citrate dextrose solution A or acid citrate de

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: Age between 30 and 70 years Diagnosis of knee osteoarthritis grade 1, 2 or 3 based on ACR clinical and radiographic criteria Knee pain for at least 6 months Visual Analogue Scale (VAS) score of at least 3 No satisfactory response to at least one conservative treatment (acetaminophen, NSAIDs, assistive devices, lifestyle modification or weight loss) At least two weeks washout period from last NSAID or corticosteroid use No history of knee injection in the last three months

Exclusion criteria

Exclusion criteria: Pregnancy or breastfeeding Inflammatory rheumatic diseases Severe heart disease Active skin infection at the injection site Use of immunosuppressive drugs Use of anticoagulants (warfarin or heparin) History of bleeding diathesis or current coagulation disorders Active low back pain with radiation to lower limbs History of knee surgery in the last 3 months Active infection or malignancy in the last 6 months Substance abuse Intra-articular corticosteroid injection in the last 3 months Intra-articular hyaluronic acid injection in the last 6 months

Design outcomes

Primary

MeasureTime frame
Pain severity measured by Visual Analogue Scale (VAS). The VAS is a 10-centimeter horizontal line with 0 meaning "no pain" and 10 meaning "worst imaginable pain". Patients mark their current pain level on this line. Timepoint: Before injection (baseline), 1 month after injection, 3 months after injection. Method of measurement: Visual Analogue Scale (VAS) - a self-administered 10-centimeter horizontal line scale. The patient places a mark on the line corresponding to their perceived pain intensity. The distance from zero to the mark is measured in millimeters, yielding a score from 0 to 100 (or 0 to 10 when converted).

Secondary

MeasureTime frame
Physical function measured by the physical function subscale of the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). This subscale contains 17 questions assessing difficulty with daily activities such as walking, climbing stairs, rising from sitting, standing, bending, and household tasks. Timepoint: Before injection (baseline), 1 month after injection, 3 months after injection. Method of measurement: Persian version of the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) physical function subscale. Each of the 17 questions is scored from 0 (no difficulty) to 4 (extreme difficulty). The total subscale score ranges from 0 to 68. Higher scores indicate worse physical function.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlireza Naeiji

Tehran University of Medical Sciences

alirezanaeiji@gmail.com+98 911 689 9200

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026