ViSiGi LUX Bariatric Sizing and Calibration System

N/AUnknownNCT06282094

Boehringer Labs LLC30 enrolled

Overview

This study investigates the new ViSiGi LUX.

ViSiGi is used during numerous gastric and bariatric procedures. The new device, ViSiGi LUX functions as the FDA-cleared ViSiGi but has the added visualization of NIR lights.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Bariatric Surgery Candidate

Eligibility

Sex: ALLMin age: 18 YearsMax age: 99 Years

Medical Language ↔ Plain English

Inclusion Criteria: * 18 years or older * able to consent * candidate for robotic bariatric surgery Exclusion Criteria: * esophageal stricture that does not allow passage of the device * conditions that would preclude gastric or bariatric surgical procedures * pregnant patients

Locations (1)

WellSpan

York, Pennsylvania, United States

RECRUITING

Outcomes

Primary Outcomes

Physician Feedback

The physician provides feedback and comments on the usability of the device. The physician will rate the device on a Likert scale. 1-7 higher score is better

Time frame: 6 months

Central Contacts

Elena Lagunilla

CONTACT

4849312338 elagunilla@boehringerlabs.com

Data from ClinicalTrials.gov

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