Comparing two methods for pain relief after minimally invasive heart surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the effectiveness of ultrasound-guided serratus anterior plane and serratus-intercostal interfascial plane blocks compared to local wound infiltration for managing postoperative pain in patients undergoing minimally invasive cardiac surgery. It is a randomized, prospective, single-blinded trial involving 60 patients, focusing on opioid consumption and pain scores post-surgery. The study aims to determine which method provides better analgesia and fewer complications during recovery.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Age 18-75 years
* Undergoing MICS with left-sided 4th-5th intercostal incision
* ASA I-III
* Informed consent provided

Exclusion Criteria:

* Coagulopathy or on anticoagulants

  * Allergy to local anesthetics or opioids
  * Local infection at block site
  * Pregnancy or lactation
  * Bilateral thoracic incisions
  * Refusal to participate

Where it's running

• Kolan International Hospital
  Istanbul, Turkey (Türkiye) Recruiting

Study contacts

• Study coordinator: Selcuk Alver, MD
• Email: alverselcuk@gmail.com
• Phone: +905435424234

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.