Comparing two pain management techniques for patients undergoing VATS
Official title: A Comparative Study of Erector Spinae Plane Block Versus Serratus Anterior Plane Block for Postoperative Analgesia After Video-assisted Thoracoscopic Surgery
Run by Ain Shams University · NCT06996691 · Data updated 2026-11-12
This study is testing which of two pain management techniques works better for people having video-assisted thoracoscopic surgery to help them recover with less pain and fewer opioids.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 70 Years |
| Sex | All |
| Enrollment | 40 (estimated) |
| Sponsor | Ain Shams University Academic / other |
| Locations | 1 site (Cairo) |
| Status | Recruiting |
| Started | May 1, 2025 |
| Main results expected | July 31, 2025 |
| Study ends | August 15, 2025 |
| Registry record updated | May 30, 2025 |
| Trial ID | NCT06996691 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients scheduled for video-assisted thoracoscopic surgery with a BMI between 18 and 40 kg/m2.
✕Probably not a fit
Patients with contraindications to regional anesthesia, chronic pain, or a history of opiate abuse 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 the Erector Spinae Plane (ESP) block compared to the Serratus Anterior Plane (SAP) block for pain management in patients undergoing video-assisted thoracoscopic surgery (VATS). The goal is to improve postoperative pain control and reduce opioid usage, which can lead to complications such as pneumonia and atelectasis. By utilizing regional anesthesia techniques, the study aims to enhance recovery and functional outcomes for patients. The study will include patients with a BMI between 18 and 40 kg/m2 and will exclude those with contraindications to regional anesthesia or pre-existing chronic pain.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management and faster recovery for patients undergoing VATS.
How similar studies have gone: Previous studies have shown promising results with regional anesthesia techniques for pain management in thoracic surgeries, indicating that this approach is both relevant and potentially effective.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * body mass index (BMI)=18 to 40 kg/m2 Exclusion Criteria: * Contraindications to regional anesthesia as bleeding disorders , allergy to local anesthetic or infection at block site * pre-existing chronic pain * history of opiate abuse * sepsis
Where it's running
-
faculty of medicine Ain Shams University
Cairo, Egypt Recruiting
Study contacts
- Study coordinator: abdallah M soudi, M.D.56k
- Email: Dr.soudi2014@med.asu.edu.eg
- Phone: +201111228925
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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.