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Comparison of ultrasound guided Suprascapular Nerve Block versus Intra- Articular Platelet Rich Plasma for Periarthritis Shoulder pain

Comparison of Efficacy of Ultrasound guided Suprascapular Nerve Block Versus Intra-Articular Platelet Rich Plasma in Periarthritis Shoulder Pain: A Randomized Controlled Trial - Nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/065537
Enrollment
60
Registered
2024-04-10
Start date
Unknown
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

Health Condition 1: M750- Adhesive capsulitis of shoulder Health Condition 2: M750- Adhesive capsulitis of shoulder

Interventions

Intervention1: USG guided Suprascapular Nerve Block: Suprascapular nerve block on affected side will be infiltrated with 10 ml of 0.5% Bupivacaine with all aseptic precautions using 21 gauge needle an

Sponsors

Uttar Pradesh University of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age more than 18 years, clinically diagnosed with periarthritis shoulder Duration of symptoms more than 4 weeks Normal anteroposterior radiographs of the glenohumeral joint

Exclusion criteria

Exclusion criteria: History of shoulder trauma, dislocation or fractures in the shoulder area, History of injection in the involved shoulder during the preceding 6 months, Bleeding disorders, Uncontrolled diabetes mellitus, Active infection at site of injection, History of allergy to local anaesthetics, Use of anticoagulant drugs in past 7 days and Affected shoulder surgery in past 1 year. 9. Patients who are pregnant or breastfeeding.

Design outcomes

Primary

MeasureTime frame
Visual Analogue ScaleTimepoint: At the time of intervention, then at 2 weeks , 6 weeks and 12 weeks post intervention.

Secondary

MeasureTime frame
Shoulder Pain and Disability Index Range Of MotionTimepoint: At the time of intervention, then at 2 weeks , 6 weeks and 12 weeks post intervention.

Countries

India

Contacts

Public ContactDr Vinay Kanaujia

Uttar Pradesh University Of Medical Sciences

vinay.kanaujia87@gmail.com8800121450

Outcome results

None listed

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