Comparıson of Analgesıc Effıcacy of Dıfferent Volumes of Serratus Posterior Superıor Intercostal Plane Block After Modıfıed Radıcal Mastectomy Surgery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-65
SponsorCumhuriyet University

About this trial

The aim of researchers is to compare the effects of three different local anesthetic concentrations and volumes on opioid consumption, postoperative analgesic efficacy, and pain scores during ultrasound-guided SPSIP blocks in patients undergoing modified radical mastectomy. Additionally, we aim to map and identify the dermatomal areas where different concentrations and volumes of SPSIP blocks provide analgesia.

Eligibility criteria

Qualifiers

The study included adult patients over 18 years of age who underwent modified radical mastectomy under general anesthesia and were classified in risk groups I-II-III according to the American Society of Anesthesiologists (ASA) risk classification.

Disqualifiers

patients with coagulopathy,

patients with signs of infection at the block application site,

patients with ASA IV

patients with known allergies to any of the study drugs,

Trial design

Treatments tested in this trial

  • Serratus Posterior Superior Intercostal Plane (SPSIP) block 40 ml of 0.125% bupivacaine
  • Serratus Posterior Superior Intercostal Plane (SPSIP) 50 ml of 0.125% bupivacaine
  • Serratus Posterior Superior Intercostal Plane (SPSIP) 30 ml of 0.25% bupivacaine

Treatment groups

90 Participants
are divided into 3 treatment groups

Sponsors and collaborators