Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
NCT06968065

Comparison of Ultrasound-Guided Serratus Combination Plane Blocks and Local Wound Infiltration for Postoperative Analgesia Management in Minimally Invasive Cardiac Surgery (MICS)

Led by İstanbul Yeni Yüzyıl Üniversitesi · Updated on 2025-05-13

60

Participants Needed

1

Research Sites

32 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This randomized, prospective, single-blinded study aims to compare the efficacy of ultrasound-guided serratus anterior plane (SAP) block combined with serratus-intercostal interfascial plane (SIP) block versus local wound infiltration (LWI) for postoperative analgesia in patients undergoing minimally invasive cardiac surgery (MICS). The primary outcome is total perioperative and postoperative opioid consumption. Secondary outcomes include postoperative pain scores (NRS), opioid-related side effects, block-related complications, and ICU stay duration.

CONDITIONS

Official Title

Comparison of Ultrasound-Guided Serratus Combination Plane Blocks and Local Wound Infiltration for Postoperative Analgesia Management in Minimally Invasive Cardiac Surgery (MICS)

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 to 75 years
  • Scheduled for minimally invasive cardiac surgery with left-sided 4th-5th intercostal incision
  • Classified as ASA physical status I to III
  • Provided informed consent to participate
Not Eligible

You will not qualify if you...

  • Having coagulopathy or taking anticoagulant medications
  • Allergy to local anesthetics or opioids
  • Local infection at the block site
  • Pregnancy or currently breastfeeding
  • Having bilateral thoracic incisions
  • Refusal to participate in the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Kolan International Hospital

Istanbul, Turkey (Türkiye)

Actively Recruiting

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Research Team

S

Selcuk Alver, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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