Clinical trial Recruiting at 1 site Interventional Ages 18 to 75

Rhomboid Intercostal Block vs Serratus Posterior Superior Intercostal Plane Block for VATS Pain

Official title: Comparison of the Effects of Ultrasound-Guided Rhomboid Intercostal Block and Serratus Posterior Superior Intercostal Plane Block on Postoperative Acute Pain in Patients Undergoing Video-Assisted Thoracoscopic Surgery

Run by Ankara City Hospital Bilkent · NCT07650877 · Data updated 2026-11-12

This study tests two regional anesthesia techniques to see which better reduces postoperative pain after video-assisted thoracic surgery in adults undergoing thoracic procedures.

More Pain, Postoperative trials

Quick facts

Study typeInterventional
Ages18 Years to 75 Years
SexAll
Enrollment90 (estimated)
SponsorAnkara City Hospital Bilkent
Academic / other
Locations1 site (Çankaya, Ankara)
StatusRecruiting
StartedJune 15, 2026
Main results expectedNovember 20, 2026
Study endsNovember 30, 2026
Registry record updatedJune 16, 2026
Trial IDNCT07650877 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18–75 undergoing elective VATS, ASA I–III, who consent to participate and have no contraindications to regional anesthesia.

Probably not a fit

Patients with contraindications to local anesthetics, bleeding disorders, infection at the block site, or inability to consent may not benefit.

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

What this trial studies

This interventional study compares rhomboid intercostal block (RIB) with serratus posterior superior intercostal plane block (SPSIPB) as part of multimodal pain management for patients undergoing elective video-assisted thoracic surgery (VATS). Eligible adults aged 18 to 75 with ASA I–III are randomized to receive one of the blocks to assess analgesic effectiveness and safety. Ultrasound-guided techniques are used, reflecting contemporary practice for regional anesthesia in thoracic surgery. The trial aims to determine which block provides superior pain relief, potential opioid-sparing benefits, and a favorable safety profile in the perioperative setting.

Why it matters

Potential benefit: If successful, one block could offer better pain control with fewer opioid needs after VATS, potentially improving recovery.

How similar studies have gone: Previous regional analgesia approaches have shown promise in reducing postoperative pain in VATS, but direct head-to-head comparisons of RIB and SPSIPB are limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients undergoing elective VATS
* Patients aged 18-75 years
* Patients with ASA (American Society of Anesthesiologists) class I-III
* Patients who have given informed consent

Exclusion Criteria:

* Patients allergic to local anesthetics
* Patients with bleeding disorders or those undergoing anticoagulant therapy
* Pregnant and breastfeeding women
* Patients with impaired consciousness, inability to communicate, or mental/cognitive impairment
* Patients who refuse block application
* Patients with infection in the area where the block will be applied

Where it's running

  • Ankara City Hospital
    Çankaya, Ankara, Turkey (Türkiye)
    Recruiting

Study contacts

Similar studies

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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.