Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorSaglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital
About this trial
This randomized, double-blind, placebo-controlled study aims to evaluate the effect of the serratus posterior superior intercostal plane (SPSIP) block on postoperative pain and opioid consumption in patients undergoing minimally invasive cardiac valve surgery via mini-thoracotomy.
Eligibility criteria
Qualifiers
Adult patients aged 18-75 years
ASA physical status I-III
Scheduled for elective minimally invasive cardiac valve surgery via mini-thoracotomy
Able to understand and use the Numeric Rating Scale (NRS)
Disqualifiers
Age >75 years
Known allergy or hypersensitivity to local anesthetics (e.g., bupivacaine)
Coagulopathy or ongoing anticoagulant therapy that cannot be discontinued
Infection at the planned block site
Trial design
Treatments tested in this trial
- Serratus Posterior Superior Intercostal Plane Block With Bupivacaine
- Serratus Posterior Superior Intercostal Plane Block With Saline
Treatment groups
90 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov