Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT07164677

Serratus Posterior Superior Plane Block for Postoperative Pain in Cardiac Surgery

Led by Ondokuz Mayıs University · Updated on 2025-09-17

50

Participants Needed

1

Research Sites

28 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of this study is to investigate the efficacy of bilateral serratus posterior superior intercostal plane (SPSIP) block on postoperative acute pain and opioid consumption in patients undergoing on-pump open-heart surgery. Postoperative outcomes including pain scores, cumulative morphine use, quality of recovery, and opioid-related side effects will be evaluated within the first 24 hours after surgery.

CONDITIONS

Official Title

Serratus Posterior Superior Plane Block for Postoperative Pain in Cardiac Surgery

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18-80 undergoing elective on-pump open-heart surgery via median sternotomy
  • American Society of Anesthesiologists (ASA) classification II-III patients
  • Patients who can use patient-controlled analgesia (PCA)
  • Patients willing to sign the informed consent form
Not Eligible

You will not qualify if you...

  • History of opioid use for more than four weeks
  • Chronic pain syndromes
  • Allergy or hypersensitivity to local anesthetics or opioids
  • Alcohol and drug addiction
  • Conditions where regional anesthesia is contraindicated
  • Failure in dermatomal examination after the block
  • Emergency surgeries and redo surgeries
  • Individuals with obstructive sleep apnea
  • Left ventricular ejection fraction less than 30%
  • Severe psychiatric illnesses limiting cooperation with pain scales
  • Pregnant and breastfeeding patients
  • Hematological disorders
  • Severe impairment of major organ function (e.g., liver or kidney)
  • Patients who cannot be extubated within 6 hours postoperatively

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

Burhan Dost

Samsun, Turkey (Türkiye), 55270

Actively Recruiting

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Research Team

B

Burhan Dost

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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