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The Effect of Ultrasonography-guided Fascial Plane Blocks in Breast Cancer Surgery Patients

NCT06419504 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 96

Last updated 2025-05-16

No results posted yet for this study

Summary

The aim of this study was to evaluate the efficacy of serratus anterior plane (SAP) block, pectoserratus plane (PECS II) block, and erector spinae plane (ESP) block on postoperative acute pain, quality of recovery and chronic pain in breast cancer surgery patients.

Conditions

Interventions

OTHER

SAP block group

US-guided SAP block is performed approximately 30 minutes before the surgery in patients undergoing breast cancer surgery in a separate regional anesthesia room with standard anesthesia monitoring.

OTHER

PECS II block group

US-guided PECS II block is performed approximately 30 minutes before the surgery in patients undergoing breast cancer surgery in a separate regional anesthesia room with standard anesthesia monitoring.

OTHER

ESP block group

US-guided ESP block is performed approximately 30 minutes before the surgery in patients undergoing breast cancer surgery in a separate regional anesthesia room with standard anesthesia monitoring.

OTHER

Control group

No intervention

Sponsors & Collaborators

  • Antalya Training and Research Hospital

    lead OTHER_GOV

Principal Investigators

  • Hafizenur O Atalay, M.D. · University of Health Sciences, Antalya Training and Researh Hospital

  • Arzu O Karaveli, M.D. · University of Health Sciences, Antalya Training and Researh Hospital

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-05-17
Primary Completion
2024-09-28
Completion
2025-02-28

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06419504 on ClinicalTrials.gov