A clinical trial to study at Sawai Man Singh Medical College, Jaipur, Rajasthan to assess the efficiency of sonography guided needle fenestration of coracohumeral ligament for the treatment of frozen shoulder patients in the frozen stage

An Interventional Study To Determine The Effectiveness Of Ultrasound Guided Needle Fenestration Of Coracohumeral Ligament For The Management Of Shoulder Adhesive Capsulitis In The Frozen Stage At Sawai Man Singh Medical College, Jaipur, Rajasthan - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/04/066466

Enrollment

Registered

2024-04-29

Start date

Unknown

Completion date

Unknown

Last updated

2024-05-27

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

Conditions

Health Condition 1: M75- Shoulder lesions

Interventions

Intervention1: An Interventional Study to Determine the Effectiveness of Ultrasound Guided Needle Fenestration of Coracohumeral Ligament for the Management of Shoulder Adhesive Capsulitis in the Froze

Eligibility

Inclusion criteria

Inclusion criteria: Those willing to give informed written consent for participating in the study Patients with shoulder adhesive capsulitis in frozen stage Normal radiological appearance

Exclusion criteria

Exclusion criteria: The patient with poorly controlled Type 2 Diabetes mellitus or HbA1c more than 7.5 The patient with skeletal abnormality of Shoulder girdle or cervical thoracic spine Patient with any shoulder weakness secondary to Trauma And Spinal cord injury Patient with bleeding disorder INR more than 1.5 and platelet count less than 1 lakh per mm3 Patient currently with blood thinner eg warfarin etc The patient with history of shoulder fracture or rotator cuff injury Those with any other medical or surgical intervention that can interfere with the diagnosis or treatment protocol Allergy or intolerance to any drug or substance being used in the study

Design outcomes

Primary

Measure	Time frame
1. Shoulder pain and disability index for pain intensity and functional disability assessment 2. Visual analog scale 3.The number of analgesics ingested per dayTimepoint: Before Intervention at the time of interview ,then follow up at baseline ,2 wks, 4 wks, 6 wks	—

Secondary

Measure	Time frame
NILTimepoint: NOT APPLICABLE	—

Countries

India

Contacts

Public ContactDr Mrinal Joshi

SMS Medical College Jaipur

dr.m.joshi@gmail.com01412561906

Outcome results

None listed

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