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Clinical Trials in Turkey / NCT06664359
Recruiting Observational

Safe Zone in Trigger Point Injection

NCT06664359 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2024-10-01
Last updated
2024-10-29

Condition(s) studied

Trigger Point Pain, Myofascial

Investigational drug(s) / intervention(s)

Ultrasound guided injection with local anaestethicUltrasound guided injection with local anaestethic

Ultrasound guided injection with local anaestethic: Volunteers will first be asked to sit on a chair with their back facing the examiner, placing their arms in a relaxed position with their head supported on a surface in front of them. The ultrasound operator will be positioned behind the volunteer. Initially, in the sitting position, volunteers will be asked to maintain normal breathing. Once an optimal ultrasound image is obtained, the image will be frozen, and measurements will be taken from the same image in sequence. The measurements to be performed are as follows: skin-fat tissue distance, skin-trapezius muscle distance, skin-rhomboid muscle distance, skin-rib distance, skin-pleura distance, and rhomboid muscle-pleura distance. These measurements, in millimeters, will be recorded in the data collection form. The same measurements will also be taken during deep inhalation and deep exhalation in the sitting position."

Ultrasound guided injection with local anaestethic: Volunteers will first be asked to lay prone position.The ultrasound operator will be positioned behind the volunteer. Initially, in the sitting position, volunteers will be asked to maintain normal breathing. Once an optimal ultrasound image is obtained, the image will be frozen, and measurements will be taken from the same image in sequence. The measurements to be performed are as follows: skin-fat tissue distance, skin-trapezius muscle distance, skin-rhomboid muscle distance, skin-rib distance, skin-pleura distance, and rhomboid muscle-pleura distance. These measurements, in millimeters, will be recorded in the data collection form. The same measurements will also be taken during deep inhalation and deep exhalation in the sitting position."

Study summary

The goal of this observational study is to define the safe distance that will reduce the risk of pneumothorax through ultrasonographic imaging measurements in both sitting and prone positions to ensure patient safety during these procedures. The main question\[s\] it aims to answer \[is/are\]:

The mean distance between the skin and pleura in sitting position during the inhalation and exhalation The mean distance between the skin and pleura in prone position during the inhalation and exhalation

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * patients diagnosed with Myofascial Pain Syndrome * patients scheduled for trigger point injections due to Myofascial Pain Syndrome. Exclusion Criteria: * under 18 years of age, * additional diseases other than Myofascial Pain Syndrome, * the presence of active infection in the interscapular area where ultrasound imaging and measurements will be performed, * lesions that disrupt skin integrity or affect subcutaneous and muscle structures such as anomalies or masses that could impair imaging quality * individuals with known lung diseases * not consent to participate in the study."

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Ankara University Department of Anesthesiology and Reanimation Ankara Turkey (Türkiye) Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06664359 on ClinicalTrials.gov ↗ ← All trials in Turkey