Clinical Trials Directory

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

TypeNameDescription
DRUGLocal levobupivacainesubmucosal 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.