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

CompletedNCT06419504
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

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.

Study details

Official title
The Effect of Ultrasonography-guided Pectoserratus Plane Block, Erector Spina Plane Block and Serratus Anterior Plane Block on Postoperative Opioid Consumption, Recovery Quality and Chronic Pain in Breast Cancer Surgery Patients
Conditions
Interventions
Sponsor
Antalya Training and Research Hospital
Start date
2024-05-17
Primary completion
2024-09-28
Sex
Female
Age range
from 18 Years to 65 Years
Results posted
No results posted in this snapshot
Countries
Turkey (Türkiye)
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * elective breast surgery (modified radical mastectomy, breast conserving surgery, simple mastectomy, axillary lymph node dissection, etc.), * 18 to 65 years old, * American Society of Anaesthesiology (ASA) score I-III * body mass index (BMI) \<32 kg/m2 Exclusion Criteria: * contraindications to the block applications * history of mental or neurological disorders * history of chronic opioid use * chronic alcoholism * substance use * treatment of chronic pain * severe liver and kidney disease * uncooperative patients * patients scheduled for bilateral mastectomy

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06419504