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Role of ultrasound guided shoulder joint hydrodistension in the management of frozen shoulder

Utility of ultrasound guided glenohumeral joint hydrodistension in the management of adhesive capsulitis: A randomized control trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/12/060642
Enrollment
40
Registered
2023-12-21
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Health Condition 1: M678- Other specified disorders of synovium and tendon

Interventions

Intervention1: Ultrasound guided hydrodistension of shoulder joint using Triamcinolone, lidocaine and normal saline.: After appropriate skin preparation, under ultrasound guidance a 24G needle will be

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients having clinically diagnosed shoulder joint Adhesive capsulitis with persistent pain and functional deficit for more than three months not resolving with conservative management.

Exclusion criteria

Exclusion criteria: 1. Patients with other causes of shoulder pain like osteoarthritis, inflammatory joint disease, rotator cuff tear and secondary adhesive capsulitis (shoulder injury or surgery). 2. Patients with underlying coagulopathies or taking anti-coagulant medications 3. Patients with local site infection 4. Patients who have received prior corticosteroid injection or have undergone arthroscopic or open capsular release surgery 5. Shoulder joint plain radiographic finding of significant glenohumeral joint arthritis - History of side effects to local anaesthetics, corticosteroids.

Design outcomes

Primary

MeasureTime frame
1. To study the improvement in range of movement (ROM) after ultrasound guided hydrodistension of glenohumeral joint. 2. To assess the improvement in shoulder pain status after hydrodistension 3. To assess the functional improvement after hydrodistension. 4. To compare the pain, range of movement & functional improvement between study & control groupTimepoint: At 4 weeks & 12 weeks

Secondary

MeasureTime frame
To record the complications if any associated with the procedure.Timepoint: At 4 weeks & 12 weeks

Countries

India

Contacts

Public ContactDr Anupama Tandon

University College of Medical Science and GTB Hospital

anupamatandon@hotmail.com8585977903

Outcome results

None listed

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