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Study identifier: NCT03876288 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Gastroparesis Outcome Longitudinal Database Enrolled Numerically

Condition: Gastroparesis  ·  Sponsor: University of Louisville

PhaseN/A
Planned participants3000
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

GOLDEN is a longitudinal database of patients with the symptoms (Sx) of gastroparesis (Gp) who were seen and recorded at the University of Louisville from 2012 and is ongoing. Patients are enrolled and followed by sequential numbers and may include legacy patients seen at other centers by some of the same team and who are reported as part of the series. Outcome relate to patients Sx, survival, quality of life and other measures as detailed below, over time. The study tracks patients regardless of treatment but specifically focuses on GI Neuromodulation (gastric electrical stimulation - GES), Immunotherapy (IVIG), and Pyloric therapies (pyloroplasty, endoscopic). If treatments were administered GOLDEN allows for examination and stratification of outcome by groups both at baseline and at follow up.

This description comes directly from the study's public registry record.

Talk to the study team

Thomas Abell, MD  ·  (502)852-6991  ·  thomas.abell@louisville.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of LouisvilleLouisville, Kentucky, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT03876288