Enhanced vs Conventional Recovery After Breast Surgery

NCT ID: NCT05931796

Last Updated: 2024-01-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

25 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-03-10

Study Completion Date

2024-01-25

Brief Summary

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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

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

Conditions

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Patient Satisfaction

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Group A

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

Group Type ACTIVE_COMPARATOR

NON-ERAS pathway

Intervention Type OTHER

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

Group B

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

Group Type ACTIVE_COMPARATOR

ERAS pathway

Intervention Type OTHER

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

Interventions

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NON-ERAS pathway

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

Intervention Type OTHER

ERAS pathway

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

Intervention Type OTHER

Eligibility Criteria

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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
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Mahmoud Saeed Ebaid

UNKNOWN

Sponsor Role collaborator

Amal Gouda Elsayed Safan

OTHER

Sponsor Role lead

Responsible Party

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Amal Gouda Elsayed Safan

lecturer of anaethesia

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Mahmoud Saeed Ebaid

Role: PRINCIPAL_INVESTIGATOR

Menoufia University

Locations

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Menoufia university

Cairo, Shibin Elkom, Egypt

Site Status

Countries

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Egypt

Other Identifiers

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3/2023ANET45

Identifier Type: -

Identifier Source: org_study_id

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