EligibleTrials

Safety and Effectiveness of Orbera365™ Intragastric Balloon System

Recruiting · NCT07062094 · Observational (researchers observe without assigning treatment) · Lead sponsor: Boston Scientific Corporation

View the official record on ClinicalTrials.gov →
Obesity

Interventions studied

Intragastric Balloon

What this trial is about

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.

Who can take part

Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)

Inclusion criteria

Exclusion criteria

Where it is running

4 locations listed.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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