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Compare the outcome of manipulation and hydrodilatation in adhesive capsulitis shoulder

Comparison of the clinical outcome between manipulation and hydrodilatation among patients with adhesive capsulitis of shoulder receiving intra-articular steroid injection - A Randomised controlled trial - nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068592
Enrollment
52
Registered
2024-06-07
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: M256- Stiffness of joint, not elsewhereclassified

Interventions

Intervention1: Intra-articular steroid Injection in hydrodilatation and manipulation: Patient will be randomized into two groups of 26 patients each by computer generated random numbers obtained afte

Sponsors

Pondicherry Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Unilateral frozen shoulder 2) Primary frozen shoulder, with no relief after physiotherapy and analgesics for a period of 3 months. 3) Loss of passive motion of the glenohumeral joint of 30 degree in at least 2 directions ( Flexion, extension, external rotation, internal rotation , abduction, adduction ) 4) Patient more than 18 years of age

Exclusion criteria

Exclusion criteria: 1)Secondary frozen shoulder 2)Patient with any injury in the ipsilateral shoulder joint 3)Rotator cuff tear / tendinitis 4)Previous history of intra articular steroid injection within three months 5)Patient with glenohumeral joint arthritis – Confirmed with xrays 6) Skin lesions over shoulder region

Design outcomes

Primary

MeasureTime frame
To compare the pain outcome using VAS score, shoulder disability by SPADI scoreTimepoint: Pain and disability is assessed on 3 weeks, 6 weeks and 12 weeks.

Secondary

MeasureTime frame
Assess the improvement in disability in patient suffering from adhesive capsulitisTimepoint: Disability is assessed on 3 weeks, 6 weeks and 12 weeks.

Countries

India

Contacts

Public ContactDr Prince Solomon

Pondicherry Institute of Medical Sciences

princesolomon_80@yahoo.com9489390335

Outcome results

None listed

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