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Comparison of Suprascapular nerve block and Hydrodilatation in frozen shoulder treatment.

Comparison of ultrasound guided suprascapular nerve block and hydrodilatation in treatment of Adhesive Capsulitis of shoulder : A randomised control trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/111868
Enrollment
30
Registered
2026-06-03
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: M750- Adhesive capsulitis of shoulder

Interventions

Intervention1: HYDRODILATATION: hydro distention patient will be paced in the lateral lying position, and the procedure will be performed via posterior approach. After appropriate sterile skin prepara

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Adult patients with diagnosed adhesive capsulitis. 2.Patients with Refractory/recurrent pain and functional deficit for more than 3 months and Not responding to conservative treatment i.e. NSAIDs or physiotherapy.

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.Patients who have shoulder joint plain radiographic finding of significant glenohumeral joint arthritis. 6.Patients who have history of side effects to local anaesthetics, corticosteroids.

Design outcomes

Primary

MeasureTime frame
1.Change from baseline of 2 scales, i.e SPADI and VAS in the 2 groups of interest (mean +/- SD} at 2 weeks, 6 weeks and 12 weeks. 2.Change from baseline of range of movements [degrees] using goniometer in both groups at 2 weeks, 6 weeks and 12 weeks.. 3.Comparison of the improvement between both groups at 2 weeks, 6 weeks and 12 weeks.. Timepoint: 1.Change from baseline of 2 scales, i.e SPADI and VAS in the 2 groups of interest (mean +/- SD} at 2 week, 6week and 12 weeks. 2.Change from baseline of range of movements [degrees] using goniometer in both groups at 2 weeks, 6 weeks and 12 weeks.. 3.Comparison of the improvement between both groups at 2 weeks, 6 weeks and 12 weeks..

Secondary

MeasureTime frame
Comparison of the patient s satisfaction level with each procedure between the 2 groups.Timepoint: 2week, 6 week, 12 week

Countries

India

Contacts

Public ContactDr Anupama Tandon

UCMS and GTB Hospital, dilshad garden, delhi 110095

anupamatandon@hotmail.com8585977903

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026