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Bilateral Erector Spinae Plane Block for Myofascial Pain Syndrome

Bilateral Erector Spinae Plane Block for Myofascial Pain Syndrome

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05565053
Enrollment
60
Registered
2022-10-04
Start date
2021-07-25
Completion date
2026-03-01
Last updated
2026-05-15

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

Conditions

Myofascial Pain Syndrome

Keywords

Erector spinae plane block, Myofascial pain syndrome, Trigger point, Algometer, Visual Analog Scale, Pain

Brief summary

The investigators aimed to evaluate the effectiveness of bilateral erector spina plane block application in myofascial pain syndrome.

Detailed description

The investigators aimed to evaluate the effectiveness of bilateral erector spina plane block application in myofascial pain syndrome by comparing trigger point injection. Group 1 received erector spinae plane block, and group 2 received trigger point injection both administered in two weekly sessions. Before the application, one week after application and one month after application the investigators aimed to compare pressure pain threshold with algometer, visual analog scale score, neck disability index score, for the two groups. Each group has 30 participants, total 60 participants included this study. The investigators planned to show that bilateral erector spinae plane block can be used as an effective and safe method in the treatment of myofascial pain syndrome, since it is easier to apply than other invasive procedures used in the treatment and has a very low complication profile.

Interventions

PROCEDUREBilateral thoracal erector spinae plane block

Bilateral upper thoracal erector spinae plane block with ultrasound

PROCEDURETrapezius muscle trigger point injection

Trapezius muscle trigger point injection

Sponsors

Istanbul University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
SINGLE (Subject)

Intervention model description

Comparing the efficacy of erector spina plan block and trigger point injection in patients with myofascial pain syndrome

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Get a myofascial pain syndrome diagnosis * No invasive procedure for myofascial pain syndrome in the last 1 month * Signing the informed consent form

Exclusion criteria

* Cervical disc herniation * Neck/shoulder, thoracal trauma or operation history * Malignancy * Kyphoscoliosis * Inflammatory diseases (Rheumatoid arthritis, ankylosing spondylitis...) * Congenital vertebral anomalies * Pregnancy * Mental, psychogenic disorder * Hematological diseases that cause bleeding and coagulation disorders * Use of antiplatelet, anticoagulant and drugs that cause bleeding tendency * Severe systemic infection such as sepsis and local infection at the intervention site * Having an allergy to any of the drugs to be used

Design outcomes

Primary

MeasureTime frameDescription
Comparison of the effectiveness of the two interventions (trigger point injection versus Erector spinae plane block) assessed by Visual analog scale (VAS):BaselineThe classic interventional treatment of myofascial back pain is trigger point injection. In addition, erector spina plan block has been applied in recent years as an interventional procedure that provides analgesia in the same region and is thought to have a long duration of action. Visual analog scale (VAS): Using a ruler, the score is determined by measuring the distance (mm) on the 10-cm line between the "no pain" anchor and the patient's mark, providing a range of scores from 0-100. A higher score indicates greater pain intensity.

Countries

Turkey (Türkiye)

Contacts

STUDY_DIRECTORHalil Çetingök

Istanbul University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 16, 2026