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Registry Evaluation of a Double Balloon Accessory Device

NCT03942965 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 165

Last updated 2020-12-11

No results posted yet for this study

Summary

This study is collecting standard of care information pertaining to the use of the accessory device and patient outcomes when this double balloon accessory device is used during endoscopic procedures in the colon.

Conditions

  • Adenomatous Polyp of Colon

Interventions

DEVICE

Double balloon accessory device

Double balloon accessory device is used during the endoscopic polypectomy procedure

Sponsors & Collaborators

  • Lumendi, LLC

    lead INDUSTRY

Principal Investigators

  • Peter Draganov, MD · University of Florida

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-22
Primary Completion
2020-12-31
Completion
2021-03-31
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 NCT03942965 on ClinicalTrials.gov