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NCT06230575 Clinical Trial

Locoregional Blocks for Breast Cancer Surgeries

Analgesia Clinical Trial

Official title:
Locoregional Blocks for Breast Cancer Surgeries

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT06230575
Other study ID # AP2312-301-072
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 1, 2024
Est. completion date July 25, 2025

Study information
Verified date February 2024
Source National Cancer Institute, Egypt
Contact Walaa Y Elsabeeny, MD
Phone +201007798466
Email Walaa.elsabeeny@nci.cu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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

Description:

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

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date July 25, 2025
Est. primary completion date June 15, 2025
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - female cancer breast patient - age from 18- 65 Exclusion Criteria: - coagulation defect - Patient refusal - abnormal kidney and or liver function tests

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• erector spinae block
Erector spinae plane block
• retrolaminar block
Retrolaminar block
• serratus anterior block
Serratus anterior plane block
• pectoral nerve block
Pectoral nerve block

Locations
Country Name City State
Egypt Walaa Y Elsabeeny Cairo

Sponsors (1)
Lead Sponsor Collaborator
National Cancer Institute, Egypt

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary time to receive first postoperative analgesic time to first dose of rescue opioid analgesic First 24 hours postoperatively
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