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A Randomised Single Blinded Study Comparing Between Ultrasound Guided Trigger Point Injection Versus Trapezius Plane Block As Treatment Modalities In Patients With Myofascial Pain Syndrome

Comparative Evaluation Of Ultrasound Guided Trigger Point Injections Versus Trapezius Plane Block In Myofascial Pain Syndrome Patients In Terms Of Pain Relief And Quality Of Life - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068647
Enrollment
64
Registered
2024-06-10
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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: M791- Myalgia

Interventions

Intervention1: Ultrasound Guided Trigger Point Injections: Under Ultrasound Guidance, using a high frequency (10-15 mHz) linear probe, the trigger points will be visualised. After anaesthetising the s

Sponsors

All India Institute Of Medical Sciences Raipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients diagnosed with myofascial pain syndrome with pain over neck or shoulders with clinically detectable trigger points 2.Patients who have given consent for study. 3.ASA grade 1 and 2 4.Patients with NRS pain scale of more than 4 out of 10 5.Patients with no motor deficits or congenital or systemic pathology 6.Patients with pain refractory to routine analgesics and physiotherapy.

Exclusion criteria

Exclusion criteria: 1.Patients who did not give consent 2.Patients who are less than age of 20 years and above 70 years of age 3.ASA grade 3 or more 4.Patients who are allergic to steroids or local anaesthetics 5.Patients who have trigger points other than neck and shoulder region 6.Patients with NRS pain scale less than 4 out of 10 7.Patients with motor deficits, congenital or systemic pathologies. 8.Patients with any local infection, coagulation abnormalities 9.Patients in whom routine analgesics have produced desired analgesic effect

Design outcomes

Primary

MeasureTime frame
Postprocedural pain intensity will be measured by NRS pain scale at every 3 weeks for first 3 visits and duration for which patient is relatively pain freeTimepoint: every 3 weeks for first 3 visits

Secondary

MeasureTime frame
Improvement in Quality of life using Quality of life ,Enjoyment and Satisfaction questionnaire- short form (Q-LES-Q-SF questionnaire)Timepoint: Every 3 weeks for 3 visits

Countries

India

Contacts

Public ContactShobika S

All India Institute Of Medical Sciences Raipur

drrampalsingh@aiimsraipur.edu.in9027335921

Outcome results

None listed

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