Locoregional Blocks for Breast Cancer Surgeries

NCT ID: NCT06230575

Last Updated: 2025-11-19

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

188 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-02-01

Study Completion Date

2025-11-07

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Breast surgeries are common operative procedures that require appropriate postoperative analgesia.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Numerous pain relief techniques, including several new regional anesthesia techniques, are available for control of acute pain after breast surgery.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Analgesia

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

erector spinae block

Erector spinae plane block on the ipsilateral operative site

Group Type ACTIVE_COMPARATOR

erector spinae block

Intervention Type PROCEDURE

Erector spinae plane block

retrolaminar block

Retrolaminar plane block on the ipsilateral operative site

Group Type EXPERIMENTAL

retrolaminar block

Intervention Type PROCEDURE

Retrolaminar block

serratus anterior block

Serratus anterior plane block on the ipsilateral operative site

Group Type EXPERIMENTAL

serratus anterior block

Intervention Type PROCEDURE

Serratus anterior plane block

pectoral nerve block II

Pectoral nerve block II on the ipsilateral operative site

Group Type EXPERIMENTAL

pectoral nerve block

Intervention Type PROCEDURE

Pectoral nerve block

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

erector spinae block

Erector spinae plane block

Intervention Type PROCEDURE

retrolaminar block

Retrolaminar block

Intervention Type PROCEDURE

serratus anterior block

Serratus anterior plane block

Intervention Type PROCEDURE

pectoral nerve block

Pectoral nerve block

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* female cancer breast patient
* age from 18- 65

Exclusion Criteria

* coagulation defect
* Patient refusal
* abnormal kidney and or liver function tests
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

National Cancer Institute, Egypt

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Walaa Youssef Elsabeeny

Assistant professor of Anesthesia, Surgical Critical care and Pain management

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Walaa Y Elsabeeny, MD

Role: PRINCIPAL_INVESTIGATOR

Assistant professor of Anesthesia, Surgical critical care and Pain Management, National Cancer Institute, Cairo University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Walaa Y Elsabeeny

Cairo, , Egypt

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

AP2312-301-072

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Pectoral Nerve Blockade in Mastectomy
NCT01943240 WITHDRAWN PHASE4