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Clinical Trial Summary

Modified radical mastectomy may be associated with severe post-operative pain, leading to chronic pain syndrome which usually requires optimal perioperative pain management.


Clinical Trial Description

Patients will be randomly into two equal groups (40 patients each) according to the adjuvant added to the local anesthetic (bupivacaine) in the serratus anterior plane block using a computer-generated random numbers concealed in sealed opaque envelopes. Group B: The patients will receive 20 ml of 0.5% bupivacaine plus 5 ml 0.9% normal saline with total volume 25 ml. Group BM: The patients will receive 20 ml of 0.5% bupivacaine plus 150 mg magnesium sulphate in 0.9% normal saline with a total volume of 25 ml. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04429893
Study type Interventional
Source Alexandria University
Contact Rehab A. Abd Elaziz, Ass. Prof.
Phone 01001073703
Email trcium2002@yahoo.com
Status Recruiting
Phase Phase 2/Phase 3
Start date January 1, 2022
Completion date September 2022

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