ClinicaliQ Trial Snapshot
- Safety and Effectiveness of Orbera365™ Intragastric Balloon System — Recruiting • Diabetes / Metabolic • NCT07062094.
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What This Trial Is Studying
This is a prospective, multi-center, standard of care registry offered to subjects in the EU only that have already agreed to receive the Orbera365™ Intragastric Balloon (IGB) System for weight loss. Subjects that agree to participate in the registry will have data reported associated with standard of care weight management visits during the time the device is implanted (in-dwell period), with an additional visit 30 days after the removal procedure. Conditions: Obesity Interventions: Intragastric Balloon Lead Sponsor: Boston Scientific Corporation Planned Enrollment: 200 participants