Visualization of the Papilla Through Use of the NuView Device in Patients With FAP

Completed

Conditions studied: Familial Adenomatous Polyposis

In brief

The goal of this observational study is to test the NuView device in participants with familial adenomatous polyposis (FAP). The main question it aims to answer is: * can the papilla be visualized using a forward-facing endoscope outfitted with the NuView device. Participants will undergo standard of care esophagogastroduodenoscopy with an additional endoscopic exam using NuView device, for which participant have given prior consent.

Key facts

Study ID

NCT05657145

Run by

Vanderbilt University Medical Center

People needed

3

Starts

2023-01-27

Expected to finish

2025-12-30

Last updated by the study team

2026-01-21

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or female, 18 to 70 years of age.
• Able to provide written informed consent.
• Have FAP

You may not qualify if…

• Females who are pregnant. As part of routine pre-operative care, all females of childbearing potential will undergo either urine or blood pregnancy testing.
• Cancer positive subjects or any patients currently undergoing any treatment or therapy to treat, cure, or mitigate cancer.
• Patients who do not meet inclusion criteria
• Patients who are unable or unwilling to provide informed consent

Where it is running

• Vanderbilt University Medical Center — Nashville, Tennessee, United States

Full record on ClinicalTrials.gov

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