Enhanced vs Conventional Recovery After Breast Surgery

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

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT05931796

Enrollment

Registered

2023-07-05

Start date

2023-03-10

Completion date

2024-01-25

Last updated

2024-01-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patient Satisfaction

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

Interventions

OTHERNON-ERAS pathway

All patients received best of care practice, with standardization of preoperative and postoperative care

OTHERERAS pathway

ERAS pathway ERAS consist of approximately 15 elements (or components) that include preoperative, intraoperative, and postoperative interventions .

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

OTHER

Masking

NONE

Eligibility

Sex/Gender

ALL

Healthy volunteers

Yes

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

Design outcomes

Primary

Measure	Time frame	Description
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.	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.

Secondary

Measure	Time frame	Description
Time of first ambulation	48 hours	hours

Other

Measure	Time frame	Description
Anesthesia recovery time	hour	minutes
Time to regular diet.	24 hours	hours
Postoperative opioid use.	48h	mg

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026