Comparison between Ultrasound guided External Oblique Intercostal Plane Block and Thoracic Erector Spinae block for Post Thoracotomy Pai

Phase 4

Recruiting

• Conditions: Surgery; Anaesthesia

• Registration Number: PACTR202302491451057
• Lead Sponsor: Dr Saad moharam

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-12-23
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Patients scheduled for Thoracic surgery aged between 21- 65 years of both genders
- ASA physical status I and II.

Exclusion Criteria

Patient refusal
presence of Infection at the injection site
patients with a history of allergy to local anesthetics
coagulopathy

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Total opioid consumption in the first 24 hours after surgery.

Secondary Outcome Measures

Name	Time	Method
•Time to first rescue analgesic demand after surgery.;•Numeric Rating Score (NRS) during rest and with coughing;•Complications occur as (hypotension, pneumothorax, Local Anaesthetic Systemic Toxicity (LAST)).