Gastroparesis Registry 3

NCT03680859 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 406

Last updated 2024-05-24

No results posted yet for this study

Summary

The purpose of this study is to create a new registry of patients with gastroparesis in order to better understand the characteristics of patients with gastroparesis and follow how their condition changes over time. The data collected may improve the understanding of the condition to enable better diagnosis and treatment.

Conditions

Sponsors & Collaborators

  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

    collaborator NIH
  • Johns Hopkins University

    collaborator OTHER
  • Massachusetts General Hospital

    collaborator OTHER
  • Temple University

    collaborator OTHER
  • University of Louisville

    collaborator OTHER
  • Wake Forest University

    collaborator OTHER
  • Texas Tech University Health Sciences Center, El Paso

    collaborator OTHER
  • Johns Hopkins Bloomberg School of Public Health

    lead OTHER

Principal Investigators

  • Henry Parkman, MD · Temple University Hospital

  • Braden Kuo, MD · Massachusetts General Hospital

  • Pankaj J Pasricha, MD · Johns Hopkins University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-24
Primary Completion
2024-05-13
Completion
2024-05-13

Countries

  • United States

Study Locations

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Entities

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 NCT03680859 on ClinicalTrials.gov