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Comparison of the efficacy of intra-articular hyaluronic acid–chondroitin injections versus hyaluronic acid in the treatment of knee osteoarthritis

Investigating the Effect of Intra-articular Injection of Hyaluronic Acid/Chondroitin Combination in Comparison with Hyaluronic Acid Injection in Patients with Knee Osteoarthritis; A Randomized Blinded Controlled Trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170608034390N19
Enrollment
100
Registered
2026-02-24
Start date
2026-02-19
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. Osteoarthritis of knee

Interventions

Intervention 1: Intra-articular injection into the affected knee joint of a syringe containing 60 mg hyaluronic acid and 90 mg chondroitin sulfate (3 mL), administered in two sessions at a 4-week inte

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients with mild to moderate knee osteoarthritis Sign the written consent form

Exclusion criteria

Exclusion criteria: Corticosteroid injection into the study knee less than 3 months ago History of septic arthritis of the knee; knee ulcer History of surgery or trauma to the knee History of Hypersensitivity reactions or allergy to hyaluronic acid or chondroitin Advanced osteoarthritis Active infections in the tissues around the knee Other inflammatory joint disorders, such as rheumatoid arthritis, psoriatic arthritis, gout, and other related conditions

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale (VAS). Timepoint: Before injection, 24 hours after each injection, 3 months after second injection. Method of measurement: Using the Visual Analogue Scale (VAS), a pain rating scale that is recorded by subjective reports. The patient records their pain level from 0 (no pain) to 10 (the most severe pain).

Secondary

MeasureTime frame
WOMAC Questionnaire. Timepoint: Before injection, 24 hours after each injection, 3 months after second injection. Method of measurement: Using the validated WOMAC index which contain 24 items include pain (5 questions about the visual pain with scoring from 0-10), stiffness (2 questions about the difficulty of movement with scoring from 0-8), and physical function (17 questions about the range of motion with scoring from 0-68).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactTayebeh Eslami

Shahid Beheshti University of Medical Sciences

t.eslami91@gmail.com+98 21 8820 0118

Outcome results

None listed

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