Clinical Feasibility Study of the BariTon™ System in Obese Patients
NCT06317129 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10
Last updated 2024-03-19
Summary
Safety evaluation of BariaTek Medical gastric restriction and biliodigestive diversion device.
Conditions
Interventions
- DEVICE
-
Endoscopic gastric restriction and biliodigestive diversion
The BariTon™ is endoscopically implanted.
Sponsors & Collaborators
-
BariaTek Medical
lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 25 Years
- Max Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-01-18
- Primary Completion
- 2024-10-31
- Completion
- 2026-01-31
Countries
- Uzbekistan
Study Locations
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