Serratus Posterior Superior Intercostal Plane Block in Minimally Invasive Cardiac Surgery
Recruiting now · Not applicable · Has a placebo group
Conditions studied: Heart Valve Disease, Postoperative Pain
In brief
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.
Key facts
- Study ID
- NCT07588230
- Run by
- Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital
- People needed
- 90
- Starts
- 2026-05-16
- Expected to finish
- 2026-10-26
- Last updated by the study team
- 2026-05-19
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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)
- Provided written informed consent
You may not qualify if…
- 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
- Chronic opioid use or chronic pain conditions
- Severe pulmonary disease affecting respiratory assessment
- Neurological or psychiatric disorders interfering with pain assessment
- Emergency surgery
- Pregnancy or breastfeeding
- Refusal to participate
Where it is running
- Fatma Acil — Diyarbakır, Outside of the US, Turkey (Türkiye) (enrolling)
Full record on ClinicalTrials.gov
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