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Recruiting Observational

The Effects of Regional Anaesthesia Techniques on Hemidiaphragm Paralysis, Postoperative Recovery Quality, Opioid Consumption, and Pain Scores

NCT07553611 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-04-21
Last updated
2026-05-11

Condition(s) studied

Regional AnaesthesiaArthroscopic Shoulder SurgeryHemidiaphragmatic ParalysisRecovery QualityOpioid ConsumptionPostoperative Pain Score

Investigational drug(s) / intervention(s)

İnterscalene block groupErector spinae plane block groupCostoclavicular block groupSupraclavivular block group

İnterscalene block group: Before the surgery, ultrasoud-guided interscalene block will be performed before the surgery under standart anaesthesia monitoring

Erector spinae plane block group: Before the surgery, ultrasoud-guided erector spinae plane block will be performed before the surgery under standart anaesthesia monitoring

Costoclavicular block group: Before the surgery, ultrasoud-guided costoclavicular block will be performed before the surgery under standart anaesthesia monitoring

Supraclavivular block group: Before the surgery, ultrasoud-guided supraclavivular block will be performed before the surgery under standart anaesthesia monitoring

Study summary

This study aims to evaluate the effects of ultrasound-guided interscalene, erector spinae plane, costoclavicular, and supraclavicular blocks on hemidiaphragmatic paralysis, postoperative recovery quality, opioid consumption, and pain scores.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * aged 18-65 years * American Society of Anaesthesiology (ASA) score I-III * body mass index (BMI) \<30kg/m2 * scheduled for elective arthroscopic surgery Exclusion Criteria: * ASA score ≥4 * BMI ≥30 kg/m2 * declining to give written informed consent * controendications for block application * history of mental or neurological disease, severe liver and/or kidney disease * history of moderate or severe pulmonary disease * abnormal preoperative chest X-ray findings * scheduled for emergency surgery

Primary outcome measure(s)

  • Hemidiaphragmatic paralysis — 30 minutes
    Diaghragmatic excursion will be assessed using a real-time M-mode ultrasound during quite breathing, deep breathing, and sniffing maneuvers (deep breathing through the nose)

Trial sites (1)

FacilityCityRegionStatus
University of Health Sciences, Antalya Training and Research Hospital Antalya Muratpaşa Recruiting
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 NCT07553611 on ClinicalTrials.gov ↗ ← All trials in Turkey