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Clinical Trials/NCT07553611
NCT07553611
Not yet recruiting
Not Applicable

Comparion of the Effects of Ultrasound-guided Interscalene Block, Erector Spinae Plane Block, Costoclavicular Block, and Supraclavicular Block on Hemidiaphragm Paralysis, Postoperative Recovery Quality, Opioid Consumption, and Pain Scores in Patients Undergoing Arthroscopic Shoulder Surgery: a Prospective Observational Trial

Antalya Training and Research Hospital1 site in 1 country88 target enrollmentStarted: April 21, 2026Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Antalya Training and Research Hospital
Enrollment
88
Locations
1
Primary Endpoint
Hemidiaphragmatic paralysis

Overview

Brief 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.

Detailed Description

Arthroscopic shoulder surgery is a significant approach to diagnosing and treating rotator cuff tears, impingement syndrome, instability, SLAP and Bankart injuries, and other shoulder disorders. Applications of this technique have become increasingly popular in recent yeras. Howeveri although arthroscopic sholuder surgery is conderered minimally invasive, it has been reported to cause moderate to severe postoperative pain, which can hinder patient recovery and rehabilitation, and potentially even extend the hospital stay. Therefore, providing an effective postoperative analgesia strategy in these patients is critical for patient comfort, mobilization, and overall recovery. Various methods are employed to managepostoperative pain in patients undergoing arthroscopic shoulder surgery, with regional techniques being the most prevalent. These regional techniques provide both intraoperative and postoperative analgesia in shoulder surgeries. The aim of this study is to evaluate the effects of ultrasound-guided four block techniques on hemidiaphragmatic paralysis, postoperative recovery quality, opioid consumption, and pain scores.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts 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

Arms & Interventions

İnterscalene group

Before the surgery, ultrasoud-guided interscalene block will be performed

Intervention: İnterscalene block group (Other)

Erector spinae plane block group

Before the surgery, ultrasoud-guided erector spinae plane block will be performed

Intervention: Erector spinae plane block group (Other)

Costoclavicular block group

Before the surgery, ultrasoud-guided costoclavicular block will be performed

Intervention: Costoclavicular block group (Other)

Supraclavicular block group

Before the surgery, ultrasoud-guided supraclavicular block will be performed

Intervention: Supraclavivular block group (Other)

Outcomes

Primary Outcomes

Hemidiaphragmatic paralysis

Time Frame: 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)

Secondary Outcomes

  • Recovery quality(5 minutes)
  • Postoperative analgesic consumption(24 hours)
  • Postoperative pain intensity(24 hours)

Investigators

Sponsor
Antalya Training and Research Hospital
Sponsor Class
Other Gov
Responsible Party
Sponsor

Study Sites (1)

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