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NOT YET RECRUITING
NCT06585371
Evaluation of a 6-month Intragastric Balloon
Sponsor: MEDICONE PROJETOS E SOLUCOES PARA A INDUSTRIA E A SAUDE LTDA
View on ClinicalTrials.gov
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.
Official title: Evaluation of the Safety and Efficacy of a 6-month Intragastric Balloon
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
46
Start Date
2024-09-15
Completion Date
2025-10-31
Last Updated
2024-09-05
Healthy Volunteers
Yes