The Effect of Ultrasonography-guided Fascial Plane Blocks in Breast Cancer Surgery Patients
NCT ID: NCT06419504
Last Updated: 2025-05-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
96 participants
OBSERVATIONAL
2024-05-17
2025-02-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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SAP block group
Before the surgery, US-guided SAP block will be performed
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.
PECS II block group
Before the surgery, US-guided PECS II block will be performed
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.
ESP block group
Before the surgery, US-guided ESP blockwill be performed
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.
Control group
No intervention
Control group
No intervention
Interventions
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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.
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.
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.
Control group
No intervention
Eligibility Criteria
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Inclusion Criteria
* 18 to 65 years old,
* American Society of Anaesthesiology (ASA) score I-III
* body mass index (BMI) \<32 kg/m2
Exclusion Criteria
* 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
18 Years
65 Years
FEMALE
No
Sponsors
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Antalya Training and Research Hospital
OTHER_GOV
Responsible Party
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Principal Investigators
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Hafizenur O Atalay, M.D.
Role: PRINCIPAL_INVESTIGATOR
University of Health Sciences, Antalya Training and Researh Hospital
Arzu O Karaveli, M.D.
Role: PRINCIPAL_INVESTIGATOR
University of Health Sciences, Antalya Training and Researh Hospital
Locations
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University of Health Sciences, Antalya Training and Researh Hospital
Antalya, Muratpaşa, Turkey (Türkiye)
Countries
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References
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Wang S, Shi J, Dai Y, Zhang J, Liu Q, Yang P, Zhu N. The effect of different nerve block strategies on the quality of post-operative recovery in breast cancer patients: A randomized controlled study. Eur J Pain. 2024 Jan;28(1):166-173. doi: 10.1002/ejp.2178. Epub 2023 Sep 1.
Fujii T, Shibata Y, Akane A, Aoki W, Sekiguchi A, Takahashi K, Matsui S, Nishiwaki K. A randomised controlled trial of pectoral nerve-2 (PECS 2) block vs. serratus plane block for chronic pain after mastectomy. Anaesthesia. 2019 Dec;74(12):1558-1562. doi: 10.1111/anae.14856. Epub 2019 Sep 19.
Other Identifiers
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6/11
Identifier Type: -
Identifier Source: org_study_id
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