About this trial
The aim is to compare the postoperative analgesic efficacy of serratus anterior plane block (SAPB) and serratus posterior superior intercostal plane block (SPSIPB) in patients undergoing mammoplasty surgery. To this end, a double-blind, randomized, controlled study has been designed. Female patients aged 18-65 years who will undergo mammoplasty surgery will be included in the study. Postoperative pain levels, opioid consumption, duration of analgesic requirement, and patient satisfaction will be evaluated in patients who receive fascial blocks for analgesic purposes.
Eligibility criteria
Qualifiers
Patients aged 18-85 years
Patients undergoing elective mammoplasty
ASA physical status I-II
Disqualifiers
Patients who refuse to participate
Mentally disabled patients
Presence of infection at the injection site
Patients with coagulopathy
Trial design
Treatments tested in this trial
- Serratus Anterior Plane Block
- Serratus Posterior Superior Intercostal Plane Block
Treatment groups
Sponsors and collaborators
Abant Izzet Baysal University
Lead sponsor
Karabuk Training and Research Hospital
Collaborator
Başakşehir Çam & Sakura City Hospital
Collaborator
Istanbul Medipol University Hospital
Collaborator