Clinical trial Recruiting at 1 site Interventional Ages 18 to 80

Comparing two pain management techniques after lung surgery

Official title: Paravertebral Block or Serratus Posterior Superior Intercostal Plane Block in Pain Management After Video-Assisted Thoracoscopic Surgery: A Randomized Controlled Clinical Trial

Run by Koç University · NCT06426706 · Data updated 2026-11-12

This study tests which of two pain management techniques works better for people having lung surgery to help them feel less pain and have fewer side effects afterward.

Quick facts

Study typeInterventional
Ages18 Years to 80 Years
SexAll
Enrollment44 (estimated)
SponsorKoç University
Academic / other
Locations1 site (Istanbul)
StatusRecruiting
StartedJanuary 3, 2025
Main results expectedFebruary 15, 2025
Study endsMarch 15, 2025
Registry record updatedJanuary 3, 2025
Trial IDNCT06426706 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 18-80 who are scheduled for video-assisted thoracoscopic surgery.

Probably not a fit

Patients with allergies to local anesthetics, chronic opioid use, or psychiatric disorders 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 clinical trial aims to compare the effectiveness of two regional anesthesia techniques, thoracal paravertebral block (TPVB) and serratus posterior superior intercostal plane block (SPSIPB), in managing postoperative pain for patients undergoing video-assisted thoracoscopic surgery (VATS). Participants will be randomly assigned to receive either TPVB or SPSIPB before their surgery. The study will evaluate total opioid consumption, pain scores, and opioid-related side effects in the 24 hours following the procedure. The goal is to determine which technique provides better pain relief and fewer side effects.

Why it matters

Potential benefit: If successful, this study could lead to improved pain management strategies for patients undergoing lung surgery, reducing opioid consumption and associated side effects.

How similar studies have gone: Previous studies have shown varying success with regional anesthesia techniques, but this specific comparison of TPVB and SPSIPB is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients between the age of 18-80 undergoing video-assisted thoracoscopic surgery

Exclusion Criteria:

* Allergy to local anaesthetics Chronic opioid use history Patients with psychiatric disorders Patients who are not open to communication Patients with chronic organ failure Patients that do not give consent Patients that need emergency surgery within the first 24 hours of the initial surgery

Where it's running

  • Koc University
    Istanbul, Turkey (Türkiye)
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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.