Opioid-Free Anesthesia in Modified Radical Mastectomy

Completed

• Conditions: Anesthesia; Surgery; Opioid Use
• Interventions: Procedure: opioid anesthesia

• Registration Number: NCT05693402
• Lead Sponsor: Etienne El Helou

Brief Summary

The aim of this study is to evaluate the efficacy of opioid-free general anesthesia for breast surgeries in female patients.

Detailed Description

Not available

Study Timeline

• Study Start: 2018-01-01
• Primary Completion: 2020-09-30
• Study Completion: 2020-12-01
• Study First Submitted: 2022-12-16
• Status Verified: 2023-01
• Study First Submitted QC: 2023-01-11
• Last Update Submitted: 2023-01-11
• Study First Posted: 2023-01-23
• Last Update Posted: 2023-01-23

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 116

Inclusion Criteria

• Patients underwenting modified radical mastectomy
• Undergoing general anesthesia

Exclusion Criteria

• Patients were excluded if they had Alzheimer's Disease, mental retardation, failure of locoregional anesthesia, contraindication for locoregional anesthesia.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Group 2 consisting of treated patients using NOFA	opioid anesthesia	Group 2 consisted of 60 patients (Mean age was 51±12 years)

Primary Outcome Measures

Name	Time	Method
Time To Extubation (TTE)	Directly intraOp	Time to Extubation in function of the two study groups
Post operative Morphone use	up to 24 hours	Patients who received Morphine at different time points in function of the two study groups

Secondary Outcome Measures

Name	Time	Method
Post Operative Nausea and Vomiting (PONV)	Up to 24hours	Patients who had PONV at different times in function of the two study groups

Trial Locations

Locations (1)

Lebanese Hospital Geitaoui-University Medical Center; 🇱🇧 Beirut, Lebanon