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Recruiting Observational

Postoperative Analgesic Effectiveness of Fascial Plane Blocks in Breast Surgery

NCT07830446 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-04-01
Last updated
2026-09-23

Condition(s) studied

Postoperative Pain

Investigational drug(s) / intervention(s)

Rhomboid intercostal plane blockSerratus posterior superior intercostal plane blockControl Group

Rhomboid intercostal plane block: A fascial plane block in which local anesthetic is injected into the plane between the rhomboid major and intercostal muscles. The treating anesthesiologist selects the technique as part of routine clinical care, and the type and dose of local anesthetic used are recorded.

Serratus posterior superior intercostal plane block: A fascial plane block in which local anesthetic is injected into the plane between the serratus posterior superior and intercostal muscles. The treating anesthesiologist selects the technique as part of routine clinical care, and the type and dose of local anesthetic used are recorded.

Control Group: Participants managed with intravenous patient-controlled analgesia as selected by the responsible anesthesiologist during routine clinical care.

Study summary

This prospective, single-center observational study will compare postoperative pain control in adults undergoing elective breast surgery. Ninety participants will be evaluated in three groups based on routine clinical care: rhomboid intercostal plane block, serratus posterior superior intercostal plane block, and control. The anesthesia method and fascial plane block will be selected by the treating anesthesiologist, and the research team will not assign participants to a group. The main outcome is the total amount of tramadol used through patient-controlled analgesia during the first 24 hours after surgery. Pain scores at rest and during movement, sensory block levels, postoperative nausea and vomiting, and block-related complications will also be recorded.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Age 18 to 80 years * American society of anesthesiologists physical status I to III * Undergoing surgery under general anesthesia * Provision of written informed consent * Scheduled for elective breast surgery Exclusion Criteria: * History of allergy to local anesthetic medications * Coagulation disorder * Body mass index greater than 40 kg/m2 * Infection at the block application site * Chronic pain syndrome * Pregnancy * Inability to communicate * Requirement for emergency surgery

Primary outcome measure(s)

  • Cumulative Tramadol Consumption During the First 24 Hours After Surgery — During the first 24 postoperative hours
    The total amount of tramadol consumed through the patient-controlled analgesia device will be recorded in milligrams at postoperative hour 24.

Trial sites (1)

FacilityCityRegionStatus
Bursa Yuksek Ihtisas Training and Research Hospital Bursa Turkey (Türkiye) Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07830446 on ClinicalTrials.gov ↗ ← All trials in Turkey