Shoulder Pericapsular Block Versus Interscalene Block in Arthroscopic Shoulder Surgery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorMarmara University

About this trial

This randomized controlled trial aims to compare the incidence of hemidiaphragmatic paralysis (HDP) following ultrasound-guided interscalene block (ISB) versus shoulder pericapsular nerve group (PENG) block in patients undergoing elective shoulder surgery under general anesthesia.

The primary objective is to determine whether the shoulder PENG block reduces the incidence of HDP compared with conventional intrafascial ISB. HDP will be assessed using ultrasound measurement of diaphragmatic excursion 30 minutes after block performance

Eligibility criteria

Qualifiers

ASA physical status I-III

Scheduled for elective shoulder surgery under general anesthesia

Able to provide informed consent

Disqualifiers

Pre-existing diaphragmatic dysfunction

Severe COPD or restrictive pulmonary disease

Neuromuscular disorders

BMI > 40 kg/m²

Trial design

Treatments tested in this trial

  • Interscalene Nerve Block
  • shoulder pericapsular nerve group block

Treatment groups

70 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators