Comparing two pain management techniques for patients undergoing VATS
A Comparative Study of Erector Spinae Plane Block Versus Serratus Anterior Plane Block for Postoperative Analgesia After Video-assisted Thoracoscopic Surgery
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
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years to 70 Years |
| Sex | All |
| Sponsor | Ain Shams University Academic / other |
| Locations | 1 site (Cairo) |
| Trial ID | NCT06996691 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this study are patients scheduled for video-assisted thoracoscopic surgery with a BMI between 18 and 40 kg/m2.
Not a fit: Patients with contraindications to regional anesthesia, chronic pain, or a history of opiate abuse may not benefit from this study.
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 performed: 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.
Eligibility criteria
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 this trial is running
Cairo
- 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
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.