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A Clinical trial to Compare the efficacy of Drug mixture- injection into Shoulder Joint via two different approaches of insertion of needle in patients affected by Frozen Shoulder done to conclude which one of the two approaches is better.

Comparative Efficacy of Hydrodilatation via Rotator Cuff interval approach versus Posterior capsule approach for Frozen Shoulder: Initial Exploration in a Randomised Control Trial Setting. - N/A

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/056161
Enrollment
60
Registered
2023-08-04
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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: USG guided Hydrodissection of Shoulder Joint Via Rotator Cuff Interval Approach.: 15 mL of hydrodissection injection mixture will consist of 5 mL of 1% lidocaine and 10 mL of normal sal

Sponsors

AIIMS Rishikesh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Limitation in the passive range of motion (ROM) OF Shoulder over 30° when compared with the contralateral side in at least two of these three movements: forward flexion, abduction, or external rotation

Exclusion criteria

Exclusion criteria: 1) Ultrasound findings of rotator cuff tears. 2) Plain radiography findings of significant glenohumeral joint arthritis 3) Accompanying cervical radiculopathy 4) Systemic inflammatory joint disease 5) Intraarticular injection into the glenohumeral joint within the past 3 months 6) History of trauma/surgery on the affected shoulders 7) Allergy to lidocaine. 8) Refusal by patient or relatives 9) Coagulopathy or patients on anticoagulants 10) Local site infection 11) Pregnancy 12) Severe Psychiatric illness

Design outcomes

Primary

MeasureTime frame
Visual analog scale for pain during motion in ultrasound guided hydrodilatation via rotator cuff interval approach group & posterior capsule approach group in Adhesive Capsulitis.Timepoint: 3 weeks 6 weeks 12 weeks—

Secondary

MeasureTime frame
SPADI scores Timepoint: 3 weeks, 6 weeks & 12 weeks post intervention.;To Compare analgesic requirements in both groups -according to Medication Quantification ScaleTimepoint: 3 weeks 6 weeks 12 weeks;To compare complications in both approachesTimepoint: Post procedure;To compare the employment status of patient.Timepoint: Pre procedure & post procedure—

Countries

India

Contacts

Public ContactDr Praveen Talawar

AIIMS Rishikesh

absy.yxes@gmail.com8452827327

Outcome results

None listed

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