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Obalon Balloon System Post-Approval Study

NCT03570034 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 201

Last updated 2020-04-30

No results posted yet for this study

Summary

The Obalon Balloon System - Post-Approval Study is a prospective, observational, and multi-center study.

Conditions

Interventions

DEVICE

Obalon Balloon System

Obalon Balloon System with a moderate intensity Weight Loss Behavioral Modification Program

Sponsors & Collaborators

  • Obalon Therapeutics, Inc.

    lead INDUSTRY

Principal Investigators

  • Shelby Sullivan, MD, FACG · University of Colorado, Denver

  • Rachel Moore, MD, FACS, FASMBS · Surgical Specialist of Louisiana

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-06-15
Primary Completion
2020-09-13
Completion
2021-03-13
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT03570034 on ClinicalTrials.gov