Registry for patients with early digestive tract neoplasms treated by endoscopic submucosal dissection

Endoscopic Submucosal Dissection Patients Registry in "Agrippa Ionescu" Hospital, Bucharest, Romania

Carol Davila University of Medicine and Pharmacy · NCT06033976

This study collects information from patients with early digestive tract growths treated with a special endoscopic technique to help improve future treatments.

Quick facts

Study typeObservational
Enrollment200 (estimated)
Ages18 Years to 100 Years
SexAll
SponsorCarol Davila University of Medicine and Pharmacy (other)
Locations1 site (Bucharest)
Trial IDNCT06033976 on ClinicalTrials.gov

What this trial studies

This registry collects data on patients with pre-neoplastic or early neoplastic lesions in the digestive tract who are treated using the endoscopic submucosal dissection (ESD) technique. Each case will be documented in an electronic record, ensuring patient consent and compliance with legal requirements. The goal is to gather comprehensive information to improve understanding and treatment outcomes for these conditions.

Who should consider this trial

Good fit: Ideal candidates include adults over 18 with epithelial or non-epithelial lesions in the esophagus, stomach, duodenum, or colon.

Not a fit: Patients under 18 or those unable to provide informed consent will not benefit from this registry.

Why it matters

Potential benefit: If successful, this registry could enhance treatment strategies and outcomes for patients with early digestive tract neoplasms.

How similar studies have performed: While registries for similar conditions exist, this specific approach using ESD for early neoplasms is relatively novel.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

* epithelial pre-neoplastic (eg. adenoma, dysplasia) lesion on the esophageal, gastric, duodenal or colorectal mucosa
* non-epithelial (eg. neuroendocrine tumor) lesion on the esophageal, gastric, duodenal or colorectal mucosa
* age \> 18 years old
* informed consent

Exclusion Criteria:

* age \< 18 years old
* no informed consent

Where this trial is running

Bucharest

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.

View on ClinicalTrials.gov →

Conditions: Neoplasm, Stomach, Neoplasm, Colorectal, Neoplasm, Esophagus, Neoplasm, Duodenal

Last reviewed 2026-05-15 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.