Trials / Recruiting
RecruitingNCT06611176
Local LevoBupivacaine for Pain Relief After Endoscopic Submucosal Dissection for Esophageal Lesions
Local Levobupivacaine for Pain Relief After Endoscopic Submucosal Dissection for Esophageal Lesions: a Randomized Controlled Trial
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 88 (estimated)
- Sponsor
- Laura Boer · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Endoscopic submucosal dissection (ESD) is commonly performed for (pre)cancerous lesions in the esophagus. Following ESD, post-procedural chest pain is seen in many patients. Studies have shown that local bupivacaine (BP) into the residual submucosal layer of the resection wound after gastric ESD could reduce post-procedural pain rates effectively. Levobupivacaine (LB) is equipotent to BP regarding analgesic effects, but has a better safety profile. No studies have been performed to evaluate the efficacy of LB after esophageal ESD to reduce pain. Therefore, we want to evaluate the effect on post-procedural pain of local application of LB during esophageal ESD.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Local levobupivacaine | submucosal injection of levobupivacaine during esophageal esad |
Timeline
- Start date
- 2024-10-24
- Primary completion
- 2025-12-31
- Completion
- 2026-03-30
- First posted
- 2024-09-24
- Last updated
- 2024-12-02
Locations
3 sites across 1 country: Netherlands
Source: ClinicalTrials.gov record NCT06611176. Inclusion in this directory is not an endorsement.