Domperidone Expanded Access Treatment Program

NCT04996134 · Status: NO_LONGER_AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2026-01-21

No results posted yet for this study

Summary

To allow the use of domperidone by patients with gastrointestinal disorders who have failed standard therapy.

Conditions

Interventions

DRUG

Domperidone Oral Product

10-30 mg of oral domperidone administered QID.

Sponsors & Collaborators

  • Wake Forest University Health Sciences

    lead OTHER

Principal Investigators

  • John Bosco, MD · Aurora BayCare Medical Center

Eligibility

Min Age
12 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

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 NCT04996134 on ClinicalTrials.gov