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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04429893
Other study ID # 0304543
Secondary ID
Status Recruiting
Phase Phase 2/Phase 3
First received
Last updated
Start date January 1, 2022
Est. completion date September 2022

Study information

Verified date July 2022
Source Alexandria University
Contact Rehab A. Abd Elaziz, Ass. Prof.
Phone 01001073703
Email trcium2002@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

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.


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date September 2022
Est. primary completion date September 2022
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 70 Years
Eligibility Inclusion Criteria: - adult female patients - American Society Of Anesthesiologists (ASA) class I or II - scheduled for elective unilateral modified radical mastectomy Exclusion Criteria - patient refusal - bilateral breast surgery - coagulation disorders - body mass index> 35 - allergy to local anaesthetics or magnesium sulphate - severe respiratory or cardiac disorders - pre-existing neurological deficits - liver or renal insufficiency

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
magnesium sulphate
assess the pain intensity of magnesium sulphate as an adjuvant to bupivacaine in serratus anterior plane block for modified radical mastectomy
bupivicaine
assess the pain intensity of magnesium sulphate as an adjuvant to bupivacaine in serratus anterior plane block for modified radical mastectomy

Locations

Country Name City State
Egypt Rehab Abd Elraof Abd Elaziz Alexandria Smouha

Sponsors (1)

Lead Sponsor Collaborator
Alexandria University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary assessment of the pain intensity Pain assessment by visual analogue scale 24 hours
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