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Traction vs. No Traction in Colonic ESD

NCT06159634 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2026-03-24

No results posted yet for this study

Summary

The goal of this prospective, randomized, controlled trial conducted at Baylor St. Luke's Medical Center is to compare the effectiveness and clinical outcomes of using a traction device in colonic endoscopic submucosal dissection (ESD) to those of using conventional ESD.

The investigators of this study hypothesize that use of the traction device will help expedite colonic endoscopic submucosal dissections.

Conditions

  • Gastrointestinal Neoplasm

Interventions

PROCEDURE

Endoscopic Submucosal Dissection

Endoscopic submucosal dissection (ESD) will be the technique used to remove target lesions.

DEVICE

Traction Device

Use of traction device to aid in removing target lesions

Sponsors & Collaborators

  • Micro-Tech Endoscopy USA

    collaborator UNKNOWN

  • Baylor College of Medicine

    lead OTHER

Principal Investigators

  • Mohamed Othman, MD · Baylor College of Medicine

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-12-05
Primary Completion
2026-12-30
Completion
2027-02-20
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06159634 on ClinicalTrials.gov