Clinical trial Recruiting at 1 site Interventional Ages 18 to 65

Comparing two pain management techniques for thoracotomy surgery

Official title: Comparison of the Effects of Paravertebral Block and Erector Spinae Plane Block on Intraoperative Opioid Consumption Using NoL Index in Thoracotomy

Run by Kocaeli University · NCT06507293 · Data updated 2026-11-12

This study is testing two different pain management techniques for patients having thoracotomy surgery to see which one helps reduce the need for opioids.

Quick facts

Study typeInterventional
Ages18 Years to 65 Years
SexAll
Enrollment60 (estimated)
SponsorKocaeli University
Academic / other
Locations1 site (Kocaeli)
StatusRecruiting
StartedAugust 1, 2024
Main results expectedNovember 1, 2025
Study endsDecember 1, 2025
Registry record updatedSeptember 4, 2025
Trial IDNCT06507293 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are patients scheduled for elective thoracotomy surgery with an ASA physical status of I-III.

Probably not a fit

Patients with spinal deformities, a BMI over 35, those weighing less than 50 kg, or those with allergies to the study medications may not benefit from this study.

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 two pain management techniques, the Paravertebral Block (PVB) and the Erector Spinae Plane Block (ESPB), in reducing opioid consumption during thoracotomy surgeries. The aim is to determine which technique provides better analgesia while minimizing the need for opioids, thereby reducing the risk of long-term adverse effects associated with high opioid use. The study will involve patients undergoing elective thoracotomy and will assess their pain management outcomes using the NoL Index. The findings could help establish a more effective pain management protocol for thoracic surgeries.

Why it matters

Potential benefit: If successful, this study could lead to improved pain management strategies that reduce opioid consumption and associated complications for patients undergoing thoracotomy.

How similar studies have gone: While there are few studies comparing these two techniques, the existing literature suggests that both PVB and ESPB can provide effective analgesia, though results are still controversial.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients undergo elective thoracotomy surgery
* ASA physical status I-III

Exclusion Criteria:

* Spinal deformities
* BMI\>35
* Patiens \<50 kg
* Allergies to study medications

Where it's running

  • Kocaeli University
    Kocaeli, Turkey (Türkiye)
    Recruiting

Study contacts

  • Principal investigator: Hadi Ufuk Yörükoğlu — Kocaeli University, Department of Anesthesiology and Reanimation
  • Study coordinator: Hadi Ufuk Yörükoğlu
  • Email: ufukyorukoglu@gmail.com
  • Phone: +902623038248

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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.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.