The ValenTx Endo Bypass System in Obese Subjects
NCT02954003 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40
Last updated 2016-11-03
Summary
The purpose of this study is to collect clinical data to support the use of the ValenTx Endo Bypass System to improve weight loss and the resolution of comorbidities in obese subjects.
Conditions
Interventions
- DEVICE
-
Endo Bypass System
Subject is implanted with the device for up to 3 years.
Sponsors & Collaborators
-
ValenTx, Inc.
lead INDUSTRY
Principal Investigators
-
Roland Maude-Griffin · ValenTx, Inc.
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2013-12-31
- Primary Completion
- 2015-10-31
- Completion
- 2018-10-31
Countries
- Canada
- Mexico
Study Locations
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