Hemi-diaphragmatic Paresis and Erector Spinae Plane Block

Completed

• Conditions: Anesthesia, Regional; Shoulder
• Interventions: Other: ESP block

• Registration Number: NCT05096377
• Lead Sponsor: Antalya Training and Research Hospital

Brief Summary

To assess the incidence of hemi-diaphragmatic paresis following ultrasound-guided erector spinae plane (ESP) block

Detailed Description

The aim of the study is to assess the effect of hemi-diaphragmatic paresis following ultrasound-guided erector spinae plane block.

Study Timeline

• Status Verified: 2021-10
• Study Start: 2021-10-07
• Study First Submitted: 2021-10-15
• Study First Submitted QC: 2021-10-15
• Study First Posted: 2021-10-27
• Primary Completion: 2022-01-31
• Study Completion: 2022-01-31
• Last Update Submitted: 2022-02-14
• Last Update Posted: 2022-02-15

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

• 18 - 85 years
• American Society of Anesthesiology (ASA) I-III
• elective shoulder surgery

Exclusion Criteria

• patient's refusal
• under 18 years of age or over 65 years of age
• ASA IV and above
• known allergy to local anaesthetic drugs
• the block cannot be applied due to bleeding disorders or localized skin infection at the injection site
• history of neurological and/or neuromucular disease
• history of severe bronchopulmonary disease
• a moderate to severe decrease in preoperative pulmonary function, or abnormality in preoperative chest radiography data (pleural effusion, pneumothorax, or hemidiaphragm elevation)

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
ESP block group	ESP block	Diaphragmatic excursion was measured using M-mode ultrasound during normal breathing, deep breathing and with the sniff manoeuvre.

Primary Outcome Measures

Name	Time	Method
incidence of hemi-diaphragmatic paresis	30 minutes	Diaphragmatic excursion was measured using M-mode ultrasound during normal breathing, deep breathing and with the sniff manoeuvre.

Secondary Outcome Measures

Name	Time	Method
intraoperative opioid consumption	2 hour	intraoperative opioid consumption will be recorded

Trial Locations

Locations (1)

Antalya Training and Research Hospital, Department of Anesthesiology and Reanimation; 🇹🇷 Muratpaşa, Antalya, Turkey