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Treatment of myofascial pain syndrome: comparison of physiologic saline interfascial injection and lidocaine trigger point injection

Comparison of the Effects of Physiologic Saline Interfascial and Lidocaine Trigger Point Injections in Treatment of Myofascial Pain Syndrome: A Double- Blind Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20190926003
Enrollment
80
Registered
2019-09-26
Start date
2019-10-03
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Myofascial pain syndrome with trigger point at upper trapezius muscle Myofascial pain syndrome Trigger point

Interventions

Ultrasound guided injection with physiologic saline 5 ml into the fascia layer between upper trapezius and levator scapulae muscles at trigger point area ,Ultrasound guided injection with 1%lidocaine
Experimental Procedure/Surgery,Active Comparator Procedure/Surgery
physiologic saline interfascial injection ,lidocaine trigger point injection

Sponsors

HRH Princess Chulabhorn College of Medical Science
Lead Sponsor
ืnone
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Diagnosis of myofascial pain syndrome in upper trapezius muscle based on Travell and Simon criteria by physiatrist 2.Having at least 1 active trigger point on upper trapezius muscle 3.No history of physical therapy or injection for myofascial pain syndrome within the past 3 months 4.No history of pain killer medication within past 48 hours 5.Able to communicate in thai language

Exclusion criteria

Exclusion criteria: 1.Bleeding tendency 2.History of neck and shoulder trauma 3.Other neck and shoulder pain condition eg. fibromyalgia, cervical radiculopathy, adhesive capsulitis 4.Allergy to lidocaine

Design outcomes

Primary

MeasureTime frame
Pain visual analogue scale baseline, 10 minutes, 2 weeks and 4 weeks after intervention Asking patient to point straight horizontal 100 mm line to define pain score

Secondary

MeasureTime frame
Neck ROM baseline, 10 minutes, 2 weeks and 4 weeks after intervention Measure neck flexion, extension, rotation, lateral bending by goniometer

Countries

Thailand

Contacts

Public ContactAnuphan Tantanatip

Chulabhorn Hospital

anuphansat@gmail.com66879896616

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026