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Comparison of effectiveness of blood products with nerve block in shoulder pain due to frozen shoulder

Comparison of efficacy of intra articular platelet rich plasma with suprascapular nerve block in periarthritis shoulder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/03/024158
Enrollment
72
Registered
2020-03-23
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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: Intra articular platelet rich plasma injection: platelet rich plasma prepared by single spin centrifugation of patients blood is injected into affected shoulder joint under ultrasonogra

Sponsors

vardhman mahavir medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Duration of symptoms >4 weeks 2.Normal anteroposterior radiograph of glenohumeral joint on affected side

Exclusion criteria

Exclusion criteria: 1. History of shoulder trauma,dislocation or fractures in the shoulder area 2. History of injection in the involved shoulder during the preceding 6 months 3.Bleeding disorders 4.Uncontrolled diabetes mellitus 5.Active infection at site of injection 6.History of allergy to local anaesthetics 7.Use of anticoagulant drugs in past 7 days 8.Affected shoulder surgery in past 1 year 9.Patients who are pregnant or breastfeeding

Design outcomes

Primary

MeasureTime frame
Comparison of efficacy of intra articular platelet rich plasma with suprascapular nerve block in terms of improvement in Visual Analogue Score for pain, Shoulder Pain and Disability Index Score and active Range of motion in involved shoulderTimepoint: at 0, 2, 6 and 12 weeks after intervention

Secondary

MeasureTime frame
comparison of efficacy of intra articular platelet rich plasma with suprascapular nerve block in periarthritis shoulder in terms of improvement in activities of daily livingTimepoint: at 12 weeks

Countries

India

Contacts

Public ContactMANISHA

Vardhman Mahavir Medical College and Safdarjung Hospital

rkwadhwa79@gmail.com9868182025

Outcome results

None listed

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