Trials / Unknown
UnknownNCT06317129
Clinical Feasibility Study of the BariTon™ System in Obese Patients
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 10 (estimated)
- Sponsor
- BariaTek Medical · Industry
- Sex
- All
- Age
- 25 Years – 60 Years
- Healthy volunteers
- Not accepted
Summary
Safety evaluation of BariaTek Medical gastric restriction and biliodigestive diversion device.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Endoscopic gastric restriction and biliodigestive diversion | The BariTon™ is endoscopically implanted. |
Timeline
- Start date
- 2024-01-18
- Primary completion
- 2024-10-31
- Completion
- 2026-01-31
- First posted
- 2024-03-19
- Last updated
- 2024-03-19
Locations
1 site across 1 country: Uzbekistan
Source: ClinicalTrials.gov record NCT06317129. Inclusion in this directory is not an endorsement.