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It is a study to see the effectiveness of Erector Spinae Plane Block in patients presenting with complain of recurring shoulder pain

Evaluation of efficacy of Erector Spinae Plane block in chronic shoulder pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/04/032684
Enrollment
30
Registered
2021-04-08
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: -

Interventions

Intervention1: Erector Spinae Plane block: Erector Spinae Plane block using USG guided technique. The patient will be made in a sitting position and a high-frequency linear-array transducer will be pl

Sponsors

Department of anaesthesiology and critical care
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of either sex, between 40-70 year of age, with chronic shoulder pain of duration more than six months not responding to at least two weeks of analgesics and conservative therapy, referred to pain clinic will be enrolled in the study

Exclusion criteria

Exclusion criteria: Patient with known contraindication for block interventions (e.g. infection at site of block, coagulopathy),history of adverse reaction to steroids and bupivacaine, uncontrolled diabtes mellitus and patients not consenting for erector spinae plane block will not be included in the study.

Design outcomes

Primary

MeasureTime frame
Pain relieveTimepoint: Pain will be assessed using visual analog scale (VAS 0-10).It will be recorded at the following interval: before the procedure, thirty minutes, one week and four weeks after the block

Secondary

MeasureTime frame
DisabilityTimepoint: disability score will be assessed by using SPADI(Shoulder Pain And Disability Index). It will be recorded at the following interval: before the procedure, thirty minutes, one week and four weeks after the block.;Range of motionTimepoint: range of motion will be recorded using goniometer.It will be recorded at the following interval: before the procedure, thirty minutes, one week and four weeks after the block

Countries

India

Contacts

Public ContactDhruv Raheja

Pt. B.D. Sharma PGIMS Rohtak

rahdruv@gmail.com8708290498

Outcome results

None listed

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