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OpenTrials
Completed

NCT Number: NCT03551379

A Double Balloon Endoscopic Platform for ESD

The purpose of this observational study is to record performance of a double balloon endolumenal interventional platform during complex colon polypectomy.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Winthrop-NYU Langone

Mineola, New York, 11501, United States

About this study

Endoscopic removal of Complex colon polyps (benign polyps >=2cm) is a technically challenging procedure. Complex benign polyps have a greater chance of becoming cancerous if not removed.

The DiLumen™ Endolumenal Interventional Platform is a non-sterile, single-use, close-fitting sleeve that fits securely over a standard endoscope to stabilize it in the large intestine, and facilitates use of the endoscope for optical visualization, diagnosis, and treatment. The device is indicated to ensure complete positioning of an endoscope in the large intestine and assist with optical visualization, diagnosis, and endoscopic treatment.

The device received 510k clearance on Dec 6, 2016. The study will evaluate performance of the device during routine, scheduled, endoscopic polyp removal for these large polyps.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects > 18 years of age
  • Subjects scheduled for endoscopic removal of suspected complex adenomatous polyps in the large intestine which are sessile or polypoid lesions ≥ 2cm, near the ileocecal valve, dentate line, over a fold, or at a flexure; and or lesions tethered to the colon wall due to previous incomplete resection
  • Subjects willing and able to give informed consent
  • Subjects who in the opinion of the Principal Investigator have no medical contraindication to endoscopic mucosal resection (EMR) or endoscopic submucosal dissection (ESD)

Exclusion criteria

  • Subjects with a contraindication to colonoscopy, including but not limited to active colitis, perforation, or stricture.
  • Subjects with a history of open or laparoscopic colorectal surgery
  • Subjects with a history of Inflammatory Bowel Disease (IBD)
  • Subjects with a suspected malignancy on polyp assessment

Treatment and study plan

Double Balloon Endoluminal Platform

Device

A DBA platform will be use din this registry study to facilitate ESD

Primary outcomes

  1. Ability to remove the complex polyp endoscopically

    Time frame: Duration of Procedure

    Was the lesion(s) able to be removed using the DiLumen Endolumenal Interventional Platform Device [Yes/No]

  2. Time taken for lesion removal

    Time frame: Intervention start time until Lesion removal

    Time for lesion(s) removal with the double balloon device after intervention begins

  3. Device or Procedural Adverse Events

    Time frame: Up to 72 hours

    Colon perforation, colon mucosal injury, excess bleeding will be recorded

Sponsors and collaborators

Lead sponsor

Lumendi, LLC

Industry

Registry information

Official study title

Single Center Prospective Evaluation Utilizing a Double Balloon Accessory Device to Facilitate Complex Endoscopic Polypectomy in Large Intestine

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Jun 11, 2018
Registry last updated
Aug 20, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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