Enhanced Recovery vs Conventional Recovery After Anesthesia for Patients Undergoing Breast Surgery

Amal Gouda Elsayed Safan1 site in 1 country25 target enrollmentMarch 10, 2023

ConditionsPatient Satisfaction

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Patient Satisfaction
Sponsor: Amal Gouda Elsayed Safan
Enrollment: 25
Locations: 1
Primary Endpoint: This study aims to explore the effectiveness and safety of the enhanced recovery after surgery (ERAS) protocol vs. traditional perioperative care programs for modified radical mastectomy.
Status: Completed
Last Updated: 2 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

the investigators hypothesize that with the use of enhanced recovery of surgery (ERAS), the postoperative hospital stay after breast surgeries is reduced and also postoperative complications are decreased.

Detailed Description

Group A NON-ERAS pathway All patients received best of care practice, with standardization of preoperative and postoperative care. Group B ERAS pathway

Registry

clinicaltrials.gov

Start Date

March 10, 2023

End Date

January 25, 2024

Last Updated

2 years ago

Study Type

Interventional

Study Design

Parallel

Sex

All

Investigators

Sponsor

Amal Gouda Elsayed Safan

Responsible Party

Sponsor Investigator

Principal Investigator

Amal Gouda Elsayed Safan

lecturer of anaethesia

Menoufia University

Eligibility Criteria

Inclusion Criteria

•• Age: 20-60 years.
•Adequate cognitive state (able to understand and collaborate)
•American society of anesthesia (ASA) I, II

Exclusion Criteria

•Patients who are:
•Uncooperative.
•Having allergy to any of the study drugs.
•Known abuse of alcohol or medication.
•Having Local infection at the site of injection or systemic infection.
•Pregnancy.
•With coagulation disorders.
•Any complicated patients

Outcomes

Primary Outcomes

This study aims to explore the effectiveness and safety of the enhanced recovery after surgery (ERAS) protocol vs. traditional perioperative care programs for modified radical mastectomy.

Time Frame: 48 hours

visual analogue scale VAS Score (a scale from 0 to 10 where 0 is interpreted as no pain, 1- 4 mild pain, 5-6 moderate pain, 7-10 severe pain) will be recorded 15 min after extubation (as soon as the patient will be alert enough to report pain)' every 1hour for the first 8hours' then every 3hours for the remaining 24 hours.