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Dopamine Antagonist
Domperidone for Gastroparesis
N/A
Waitlist Available
Led By George L. Arnold, MD
Research Sponsored by Arnold, George, M.D.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up domperidone will be prescrided as long as patients benefit from taking it.
Awards & highlights
Study Summary
The purpose of this study is to prescribe oral domperidone for subjects with gastrointestinal disorders who have failed or suffered adverse effects from standard medical treatment.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ domperidone will be prescrided as long as patients benefit from taking it.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~domperidone will be prescrided as long as patients benefit from taking it.
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Improvement of symptoms for patients with gastrointestinal disorders who have failed or suffered adverse effects from standard medical treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: DomperidoneExperimental Treatment1 Intervention
All eligible subjects will receive domperidone in an open label, single group assignment.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Domperidone
FDA approved
Find a Location
Who is running the clinical trial?
Arnold, George, M.D.Lead Sponsor
George L. Arnold, MDPrincipal InvestigatorGeorge L. Arnold, MD, FACP
Frequently Asked Questions
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