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OpenTrials
Completed

NCT Number: NCT06230575

Locoregional Blocks for Breast Cancer Surgeries

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

Completed

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Key information

Age range

18 year–65 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Walaa Y Elsabeeny

Cairo, 11796, Egypt

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • female cancer breast patient
  • age from 18- 65

Exclusion criteria

  • coagulation defect
  • Patient refusal
  • abnormal kidney and or liver function tests

Treatment and study plan

erector spinae block

Procedure

Erector spinae plane block

retrolaminar block

Procedure

Retrolaminar block

serratus anterior block

Procedure

Serratus anterior plane block

pectoral nerve block

Procedure

Pectoral nerve block

Primary outcomes

  1. time to receive first postoperative analgesic

    Time frame: First 24 hours postoperatively

    time to first dose of rescue opioid analgesic

Sponsors and collaborators

Lead sponsor

National Cancer Institute, Egypt

Other

Registry information

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Jan 30, 2024
Registry last updated
Nov 19, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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