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To study the effect of continuous supra scapular nerve block under ultrasound guidance in patients with chronic shoulder pain

To study the efficacy of ultrasound guided continuous supra scapular nerve block in patients with chronic shoulder pain - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/061067
Enrollment
45
Registered
2024-01-02
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

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 Health Condition 2: O- Medical and Surgical Health Condition 3: O- Medical and Surgical

Interventions

Intervention1: Ultrasound guided continuous suprascapular nerve block: Eligible patients will be assesed for intensity of pain by Numerical rating scale (NRS),shoulder pain and range of motion throug

Sponsors

JSS Academy Of Higher Education And Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of either sex between 18 to 80 years of age with chronic shoulder pain Shoulder pain with duration of more than 3 months Pain and Restriction of range of motion in one shoulder Patients with shoulder pain NRS more than or equal to 4 patients not responding to conservative management

Exclusion criteria

Exclusion criteria: Patients with coagulopathy and or on anticoagulants Infection at the site of injection Hypersensitivity to local anaesthetics Malignancy as a cause of shoulder pain Evidence of significant progressive motor deficit Fractures around shoulder and clavicle

Design outcomes

Primary

MeasureTime frame
To study the efficacy of ultrasound guided continuous supra scapular nerve block for chronic shoulder pain regarding the intensity of pain using NRS scaleTimepoint: Pain intensity assesment will be done pre-procedure ,immediate post-procedure,and at intervals of 5 days,2,4,12 and 24 weeks .

Secondary

MeasureTime frame
To assess shoulder pain and range of motion by shouder pain and disability index (SPADI) To determine patient satisfaction using Global perceived index (GPI)Timepoint: SPADI and GPI assesment Will be done pre-procedure ,immediate post-procedure,and at intervals of 5 days,2,4,12 and 24 weeks .

Countries

India

Contacts

Public ContactDr Pratibha Matche

JSS Academy of Higher Education and Research

pmatche@gmail.com9845055453

Outcome results

None listed

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