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NCT05073900 Clinical Trial

Comparison of the Efficacy of Rhomboid Intercostal Block and Erector Spinal Plane Block on Myofascial Pain Syndrome

Myofascial Pain Syndrome Clinical Trial

Official title:
Comparison of the Efficacy of Ultrasound Guided Rhomboid Intercostal Block and Erector Spinal Plane Block on Lower Cervical and Interscapular Myofascial Pain Syndrome

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05073900
Other study ID # 107/29
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 10, 2021
Est. completion date October 24, 2021

Study information
Verified date November 2021
Source Diskapi Teaching and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators evaluate the effect of Ultrasound guided Rhomboid Intercostal Block and Erector Spinal Plane Block on lower cervical and inter scapular Myofascial Pain

Description:

Myofascial pain syndrome (MPS) is the most common cause of musculoskeletal pain and its prevalence in the population is reported to be 21-30%. In this study, the investigators compare the effect of two regional anesthesia block techniques with the ultrasound guidance.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date October 24, 2021
Est. primary completion date September 10, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Complaint of myofascial pain - Pain that is rated at least 3 on a numerical rating scale (NRS, 0 = no pain, 10 = the worst pain) Exclusion Criteria: - pregnancy - presence of coagulopathy, or the use of anticoagulants - a history of surgery on the block area - allergic to bupivacaine - decline to participate

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Rhomboid intercostal block
two regional anesthesia block techniques are applied

Locations
Country Name City State
Turkey Diskapi Yildirim Beyazit Training and Research Hospital Ankara

Sponsors (1)
Lead Sponsor Collaborator
Diskapi Teaching and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Numerical Rating Scale (NRS) Pain Score Change The 11-point NRS consists of numbers between 0 and 10 where 0 indicates "no pain" and 10 indicates "maximum pain." The patient is instructed to identify one number between 0 and 10, which is best representative of their pain intensity. Change from baseline to minutes 30, day 1, week 1, 2, 4, 6 after the block
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