Comparing pain relief methods after thoracotomy surgery
Continue Erector Spinae Plane Block Versus Continue Erector Spinae Block Combined With Serratus Anterior Plane Block in Patients Undergoing Thoracotomy
This study is testing two different pain relief methods for people having thoracotomy surgery to see which one helps them feel better and recover faster.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | Bursa City Hospital Government |
| Locations | 1 site (Bursa) |
| Trial ID | NCT06685445 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of two pain management techniques, the Erector Spinae Plane Block (ESPB) and the combination of ESPB with the Serratus Anterior Plane Block (SAPB), in patients who have undergone thoracotomy. Thoracotomy is known to cause significant postoperative pain, which can lead to serious complications such as respiratory issues. By comparing these two methods, the study seeks to determine which approach provides better analgesia and improves recovery outcomes. The study will involve patients aged 18-80 with ASA classifications I-III scheduled for thoracotomy, excluding those with certain psychiatric or neurological conditions.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18-80 with ASA classifications I-III scheduled for thoracotomy.
Not a fit: Patients with psychiatric or neurological disorders affecting pain perception or those with contraindications to regional anesthesia 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 thoracotomy, enhancing recovery and reducing complications.
How similar studies have performed: Previous studies have shown promising results with regional anesthesia techniques like ESPB and SAPB, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients with ASA classification I-III * Aged 18-80 years * Who will be scheduled for thoracotomy Exclusion Criteria: * Those with psychiatric-neurological diseases that may affect pain perception * Regular users of antipsychotics, antidepressants * Allergic to any of the drugs specified in the protocol * Presence of contraindications to regional anesthesia (infection at the site of the block, bleeding diathesis, etc.)
Where this trial is running
Bursa
- Bursa City Hospital — Bursa, Turkey (Recruiting)
Study contacts
- Study coordinator: Mursel Ekinci, Assocprof MD
- Email: drmurselekinci@gmail.com
- Phone: +905067137596
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.