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.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 75 Years |
| Sex | All |
| Enrollment | 90 (estimated) |
| Sponsor | Ankara City Hospital Bilkent Academic / other |
| Locations | 1 site (Çankaya, Ankara) |
| Status | Recruiting |
| Started | June 15, 2026 |
| Main results expected | November 20, 2026 |
| Study ends | November 30, 2026 |
| Registry record updated | June 16, 2026 |
| Trial ID | NCT07650877 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
- Study coordinator: Emine Nilgün Zengin, Associate Professor
- Email: nilbavullu@gmail.com
- Phone: 00905063370548
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.