Evaluation of a 6-month Intragastric Balloon
NCT06585371 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 46
Last updated 2024-09-05
Summary
Post-market observational, adaptive, single-arm clinical study to evaluate the percentage of total weight loss after treatment with an intragastric balloon. Patients will be followed for 6 months after the device is installed.
Conditions
- Obesity and Overweight
Sponsors & Collaborators
-
MEDICONE PROJETOS E SOLUCOES PARA A INDUSTRIA E A SAUDE LTDA
lead OTHER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2024-09-15
- Primary Completion
- 2025-03-15
- Completion
- 2025-10-31
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