Evaluation of a 6-month Intragastric Balloon

NCT06585371 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 46

Last updated 2024-09-05

No results posted yet for this study

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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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06585371 on ClinicalTrials.gov