Short and Long Term Clinical and Patient-Reported Outcomes Associated With Intragastric Balloon Placement in Patients With Nonalcoholic Fatty Liver Disease

Part of paid clinical trials in Dallas, Texas.

Sponsor
Methodist Health System
Study ID
NCT07493967
Status
Enrolling By Invitation

Conditions

  • NAFLD

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Study Details

This study aims to enroll a robust cohort of NAFLD patients who undergo Intragastric Balloon placement through a multidisciplinary program approach to evaluate clinical and patient-reported outcomes for at least one-year post-placement.

Key Dates

Start date
Feb 23, 2024
Status verified
Mar 2026
Primary completion
Dec 31, 2026
Completion
Feb 28, 2027

Study Design

Enrollment
200 participants (estimated)

Primary Outcome Measure

Changes in Weight [ Time Frame: through study completion, up to 18 months ]

Locations (1)

FacilityCityStateZIPSite coordinators
Methodist Dallas Medical CenterDallasTexas75203-

Find similar trials in Dallas, TX

By research site
Methodist Dallas Medical Center· Dallas, TX

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