RecruitingNot ApplicableNCT06611176

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


Sponsor

Laura Boer

Enrollment

88 participants

Start Date

Oct 24, 2024

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Local levobupivacaine for people with endoscopic submucosal dissection and levobupivacaine. The study is currently recruiting participants at 3 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGLocal levobupivacaine

submucosal injection of levobupivacaine during esophageal esad


Locations(3)

UMCG

Groningen, Netherlands

St Antonius Hospital

Nieuwegein, Netherlands

UMCU

Utrecht, Netherlands

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NCT06611176


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