Comparing two pain management techniques for lung surgery
Comparison of Serratus Posterior Superior Interfacial Plane Block vs Serratus Anterior Plane Block on Postoperative Analgesia in Patients Underwent Video-Assisted Thoracoscopic Surgery: A Randomized, Prospective, Controlled Study
This study is trying to see if one pain management technique works better than another for helping people feel less pain after lung surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Sponsor | Medipol University Academic / other |
| Locations | 1 site (Istanbul, Bagcilar) |
| Trial ID | NCT06546839 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the effectiveness of the serratus posterior superior interfacial plane block (SPSIPB) compared to the serratus anterior plane block (SAPB) for managing postoperative pain in patients undergoing video-assisted thoracic surgery (VATS). The study aims to determine which analgesic technique provides better pain relief and reduces the risk of pulmonary complications after surgery. Participants will be monitored for pain levels and any potential side effects associated with the analgesia methods used. The trial focuses on patients classified as ASA I-III who are scheduled for VATS under general anesthesia.
Who should consider this trial
Good fit: Ideal candidates for this study are patients classified as ASA I-III who are scheduled for video-assisted thoracic surgery.
Not a fit: Patients with a history of bleeding disorders, those on anticoagulant therapy, or individuals with allergies to local anesthetics or opioids may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for patients undergoing lung surgery, enhancing recovery and reducing complications.
How similar studies have performed: Other studies have shown promising results with similar regional analgesia techniques, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * American Society of Anesthesiologists (ASA) classification I-III * Scheduled for VATS under general anesthesia Exclusion Criteria: history of bleeding diathesis, receiving anticoagulant treatment, known local anesthetics and opioid allergy, infection of the skin at the site of the needle puncture, pregnancy or lactation, patients who do not accept the procedure
Where this trial is running
Istanbul, Bagcilar
- Istanbul Medipol University Hospital — Istanbul, Bagcilar, Turkey (Recruiting)
Study contacts
- Study coordinator: Bahadir Ciftci, Assoc Prof, MD
- Email: bciftci@medipol.edu.tr
- Phone: +905343736865
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.