- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05565053
Bilateral Erector Spinae Plane Block for Myofascial Pain Syndrome
May 12, 2026 updated by: Halil Cetingok, Istanbul University
The investigators aimed to evaluate the effectiveness of bilateral erector spina plane block application in myofascial pain syndrome.
Study Overview
Status
Completed
Conditions
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.
Study Type
Interventional
Enrollment (Actual)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Istanbul, Turkey (Türkiye), 34104
- Istanbul University Istanbul Faculty of Medicine
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Bilateral Erector Spinae Plane Block
|
Bilateral upper thoracal erector spinae plane block with ultrasound
|
|
Active Comparator: Trigger Point Injection
Trapezius muscle Trigger Point Injection
|
Trapezius muscle trigger point injection
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Comparison of the effectiveness of the two interventions (trigger point injection versus Erector spinae plane block) assessed by Visual analog scale (VAS):
Time Frame: Baseline
|
The 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.
|
Baseline
|
|
Comparison of the effectiveness of the two interventions (trigger point injection versus Erector spinae plane block) assessed by Visual analog scale (VAS):
Time Frame: 1. month
|
The 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.
|
1. month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Halil Çetingök, Istanbul University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 25, 2021
Primary Completion (Actual)
January 1, 2025
Study Completion (Actual)
March 1, 2026
Study Registration Dates
First Submitted
August 5, 2022
First Submitted That Met QC Criteria
October 3, 2022
First Posted (Actual)
October 4, 2022
Study Record Updates
Last Update Posted (Actual)
May 15, 2026
Last Update Submitted That Met QC Criteria
May 12, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2019/725
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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Alexandria UniversityRecruiting