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Effect Of Prolotherapy and Steroid in Frozen Shoulder

Comparative Study Between Ultrasound guided Shoulder Intraarticular Corticosteroid versus Suprascapular Nerve Block With 5 percent Dextrose versus Steroid with Physical Exercises in Grade II and III Adhesive Capsulitis - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/096935
Enrollment
192
Registered
2025-11-06
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Intraarticular corticosteroid : 1mL triamcinolone acetonide 40 mg per mL mixed with 2 mL of 1 percent lignocaine injection in glenohumeral joint Control Intervention1: SSNB suprascapul

Sponsors

NRS Medical College Kolkata
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Pain for at least 3 months 2.VAS at least 5 3.Clinical diagnosis of Periadhesive capsulitis with restricted active and passive range of motion in external rotation 4.Inadequate response to conventional treatment

Exclusion criteria

Exclusion criteria: 1.Intraarticular injection or surgery on the affected shoulder within last 6 months 2.Full thickness rotator cuff tear advanced AC GH arthritis 3.Hemiplegic shoulder pain 4.Rheumatoid or other systemic inflammatory arthritis 5.Hypothyroidism Diabetes Complex regional pain syndrome 6.Known bleeding disorder or anticoagulant use 7.Allergy to steroid lignocaine or dextrose 8.Local or systemic infection 9.Cervical radiculopathy myelopathy 10.Pregnancy lactation 11.Immunocompromised state

Design outcomes

Primary

MeasureTime frame
VAS Visual Analogue ScaleTimepoint: VAS at baseline VAS after 1 week VAS after 4 weeks VAS after 12 weeks

Secondary

MeasureTime frame
SPADI pain shoulder pain & disability indexTimepoint: baseline 1 week 4 weeks 12 weeks;SPADI disabilityTimepoint: baseline 1 week 4 weeks 12 weeks;SPADI totalTimepoint: baseline 1 week 4 weeks 12 weeks

Countries

India

Contacts

Public ContactPartha Pratim Das

NRS Medical College Kolkata

drppdaspmr74@gmail.com9433943719

Outcome results

None listed

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