Serratus Anterior Block and Erector Spinae Block in Postoperative Analgesia

• Status: Completed
• Trial end date: 2021-02-28
• Target enrollment: 0
• Participant gender: All

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.

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: National Cancer Institute, Egypt
• Treatments: Bupivacaine

Criteria

Inclusion Criteria:

• Patients with class II physical status (American Society of Anaesthesiologists) ,

• Age between 18-70 years,

• Scheduled for thoracic cancer surgery

Exclusion Criteria:

• Patient refusal.

• Local infection at the site of the block.

• Cardiac dysfunction (ejection fraction <45%).

• Significant respiratory disorders.

• Preexisting neurological or psychiatric disease.

• Allergy to one of the study drugs.

• Pregnancy.

• Coagulopathy