Comparing different anesthesia techniques for pain relief in thoracoscopic sympathectomy patients
A Randomized Clinical Trial Comparing Transverse Thoracic Plane Block, Midpoint Transverse Process Plane to Pleura Block and Erector Spinae Plane Block for Analgesia in Patients Undergoing Thoracoscopic Sympathectomy
This study is testing which of three different anesthesia methods can provide the best pain relief for patients having surgery to treat excessive sweating or certain blood flow issues.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Tanta University Academic / other |
| Locations | 1 site (Tanta, El-Gharbia) |
| Trial ID | NCT06987110 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of three different regional anesthesia techniques—transversus thoracic muscle plane block (TTPB), mid-transverse to pleura block (MTPB), and erector spinae plane block (ESPB)—for providing postoperative analgesia in patients undergoing thoracoscopic sympathectomy. The aim is to determine which technique offers the best pain relief following this surgical procedure, which is commonly performed for hyperhidrosis and certain vascular conditions. The study involves patients aged 18 to 65 who are in good health and scheduled for the surgery, while excluding those with specific contraindications.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 to 65 who are scheduled for thoracoscopic sympathectomy and are in good physical health.
Not a fit: Patients with coagulopathy, chronic pain, or allergies to local anesthetics 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 thoracoscopic sympathectomy.
How similar studies have performed: Other studies have shown promising results with similar regional anesthesia techniques, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age from 18 to 65 years. * Both sexes. * American Society of Anesthesiology (ASA) physical status I-II. * Scheduled for thoracoscopic sympathectomy Exclusion Criteria: * Coagulopathy. * History of opiate abuse. * Pre-existing chronic pain. * Allergy to local anesthetics or analgesics. * Infection at the site of injection. * Mental or neurological disorders. * Pregnancy
Where this trial is running
Tanta, El-Gharbia
- Tanta University — Tanta, El-Gharbia, Egypt (Recruiting)
Study contacts
- Study coordinator: Mahmoud A Abdalsattar Elmohasseb, MD
- Email: mahmoud.elmahsab@med.tanta.edu.eg
- Phone: 00201023912236
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.