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A clinical trial to compare the effects of Intraarticular hylan g-f 20, dextrose, ozone and combination of dextrose & ozone in patients with osteoarthritis knee.

Comparative study of intraarticular hylan g-f 20, intra articular dextrose prolotherapy, intra articular ozone and intra articular ozone with dextrose in knee osteoarthritis for pain relief: a randomised controlled trial

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/06/008734
Enrollment
60
Registered
2017-06-01
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Knee osteoarthritis

Interventions

Intervention1: hylan g-f 20, dextrose, ozone, dextrose with ozone: high molecular weight hylan g-f 20 6 ml intra-articular once dextrose 12.5% 10 ml intra-articular once per week for 5 weeks ozone 15

Sponsors

ESI Institute of Pain Management
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Pain in the knee Kellgren â?? Lawrence grade I,II,III on PA knee radiograph, and grade IV not willing to surgery Age 50 to 75 years. Any THREE of the following: a) Less than 30 minutes of morning stiffness. b) Crepitus on active movement. c) Bony tenderness. d) Bony enlargement. e) No palpable warmth of synovium.

Exclusion criteria

Exclusion criteria: Systemic disease On anticoagulants Knee pain/ swelling due to inflammation, infection etc. Previous intra articular injection. Use of opioid analgesics. Intra articular fluid accumulation. Patients taking opioid analgesics.

Design outcomes

Primary

MeasureTime frame
Pain in Numeric Rating Scale ScoreTimepoint: Day 0 and 2 months after the completion of treatment course

Secondary

MeasureTime frame
function by Western Ontario and McMaster University Arthritis Index (WOMAC) scoreTimepoint: day 0 and 2 months after completion of treatment course;Joint space in standing Xray of affected knee jointTimepoint: day 0 and 2 months after the completion of treatment course

Countries

India

Contacts

Public ContactDr Subrata Goswami

ESI Institute of Pain Management

drsgoswami@gmail.com9830430430

Outcome results

None listed

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