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Ozone and Adhesive Capsulitis

Efficacy of Intra-articular injection of Ozone vs Intra-articular injection of Corticosteroids on Pain and Range of motion of shoulder joint in the patients with Adhesive Capsulitis (A randomized clinical trial)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20100718004409N17
Enrollment
60
Registered
2025-09-02
Start date
2025-09-20
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Adhesive capsulitis (frozen shoulder). Adhesive capsulitis of shoulder

Interventions

Intervention 1: First group: Intra-articular injection of 1cc triamcinolone (40mg) into the glenohumeral joint + home exercise program after 48h. Intervention 2: Second group: Intra-articular injectio

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: Age over 40 Shoulder pain that has lasted at least 6 weeks Reduced active and passive range of motion of the shoulder

Exclusion criteria

Exclusion criteria: Evidence of tendon calcification on radiographs Presence of systemic inflammatory diseases involving the shoulder joint, such as Rheumatoid Arthritis Receiving supportive treatments such as physiotherapy, acupuncture, biologic injections, and corticosteroid injections within the past 6 weeks History of shoulder surgery within the past year Contraindication of MRI Contraindication of corticosteroid injections History of malignancy or metastasis in the shoulder and adjacent areas

Design outcomes

Primary

MeasureTime frame
Shoulder pain. Timepoint: 1, 3 and 6 months after starting intervention. Method of measurement: Visual Analog Scale.;Shoulder Range Of Motion. Timepoint: 1, 3 and 6 months after starting intervention. Method of measurement: Goniometer.

Secondary

MeasureTime frame
Shoulder function. Timepoint: 1, 3, and 6 months after starting intervention. Method of measurement: Disabilities of the Arm, Shoulder and Hand and Western Ontario Rotator Cuff questionnaires.;Analgesic use. Timepoint: 1, 3, and 6 months after starting intervention. Method of measurement: Interview.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Parisa Nejati

Iran University of Medical Sciences

parisanejati@iums.ac.ir+98 21 6435 2446

Outcome results

None listed

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