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Serratus Anterior Block and Erector Spinae Block in Postoperative Analgesia

Postoperative Analgesia Clinical Trial

Official title:
Evaluation of the Effect of Serratus Anterior Block and Erector Spinae Block on Postoperative Analgesia in Thoracic Surgeries

Clinical Trial Summary

90 patients scheduled for thoracic cancer surgeries, allocated in 3 groups for serratus anterior block and erector spinae block and control group. during anaesthesia:total intraoperative fentanyl required will be recorded. After surgery, all patients will be connected to PCA device containing morphine solution, the amount of morphine consumed during the first 24 hours will be recorded.

Clinical Trial Description

90 patients scheduled for thoracic cancer surgeries, allocated in 3 groups for serratus anterior block (SAB) and erector spinae block (ESB) and control group. During anaesthesia: total intraoperative fentanyl required will be recorded. After surgery, all patients will be connected to PCA device containing morphine solution, the amount of morphine consumed during the first 24 hours will be recorded. Other secondary outcomes are: numerical rating scales and postoperative pulmonary functions. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04579302
Study type Interventional
Source National Cancer Institute, Egypt
Contact
Status Completed
Phase N/A
Start date November 1, 2020
Completion date February 28, 2021
View Details
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