Pain control methods for patients undergoing esophagectomy
Official title: A Randomized Controlled Trial Comparing Local Intercostal Nerve Blocks, Cryo-ablation Plus Intercostal Nerve Blocks, and Serratus Plane Catheter Plus Intercostal Nerve Blocks After Minimally Invasive Esophagectomy
Run by Swedish Medical Center · NCT05906134 · Data updated 2026-11-12
This study is testing three different ways to manage pain for patients having minimally invasive esophagectomies to see which one works best.
Quick facts
| Phase | Phase1; Phase2 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 30 (estimated) |
| Sponsor | Swedish Medical Center Academic / other |
| Locations | 1 site (Seattle, Washington) |
| Status | Recruiting |
| Started | April 26, 2022 |
| Main results expected | April 2026 |
| Study ends | February 2027 |
| Registry record updated | July 23, 2025 |
| Trial ID | NCT05906134 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adult patients scheduled for a minimally invasive esophagectomy at Swedish Medical Center.
✕Probably not a fit
Patients under 18, those unable to consent, or individuals with chronic pain requiring daily narcotics 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 pilot randomized controlled trial aims to compare three different pain control methods in patients undergoing minimally invasive esophagectomies. Participants will be randomly assigned to receive either intercostal nerve blocks, cryo-ablation combined with intercostal nerve blocks, or serratus plane catheter plus intercostal nerve blocks. The study will enroll a total of 30 patients, who will be monitored throughout their hospital stay and followed up for up to one year post-surgery to assess pain management effectiveness and postoperative complications.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for patients undergoing esophagectomy, enhancing recovery and quality of life.
How similar studies have gone: Previous studies have shown varying success with nerve block techniques for postoperative pain management, but this specific combination approach is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: All adult individuals who undergo an esophagectomy with an intended minimally invasive approach of the chest at Swedish Medical Center-First Hill. These approaches include: * 3-hole with R video-assisted thoracoscopic surgery (VATS) * Ivor Lewis R VATS Exclusion Criteria: * Age \<18 * Unable to consent * Additional surgical procedures planned * Patients with previous thoracic surgery * Patient with chronic pain on a daily regimen of narcotics * Non-English speaking * Contraindications to neuraxial anesthesia (ongoing anticoagulation, anticipated post-operative therapeutic anticoagulation, spinal cord stimulators, anatomic abnormalities preventing epidural placement)
Where it's running
-
Swedish Cancer Institute
Seattle, Washington, United States Recruiting
Study contacts
- Principal investigator: Brian Louie, M.D. — Swedish Cancer Institute
- Study coordinator: Brian Louie, M.D.
- Email: brian.louie@swedish.org
- Phone: (206) 215-6800
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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.