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Analgesic Efficacy of Ultrasound Guided Erector Spinae Block for Modified Radical Mastectomy

Pain, Postoperative Clinical Trial

Official title:
Analgesic Efficacy of Magnesium Sulphate as an Adjuvant to Levo-bupivacine in Ultrasound Guided Erector Spinae Plan Block for Modified Radical Mastectomy

Clinical Trial Summary

To compare the analgesic efficacy of dexmedetomidine and magnesium sulphate as adjuvants to levobupivacaine in erector spinae plane block in modified radical mastectomy surgery for acute and chronic pain management.

Clinical Trial Description

3 groups. Group (C) / (I):20 patient (control group) : Patients will receive 20 ml 0.25% levobupivacaine into the interfascial plane below erector spinae muscle at level of T5. Group (D)/ (II) :20 patient (Dexmetonidine group) : Patient will receive 20ml 0.25% levobupivacaineas above + 1μ/kg dexmedetomidine. Group (M) / (III) : 20 patient (magnesium slphate group) : Patient will receive 20ml 0.25% levobupivacaineas above + 0.7 mg/kg MgSo4 . The patient, the anesthesiologist who administered the drugs, and the data collector will be blinded to the study drugs. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04732364
Study type Interventional
Source South Egypt Cancer Institute
Contact
Status Enrolling by invitation
Phase Phase 2/Phase 3
Start date April 30, 2018
Completion date February 28, 2021
View Details
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