Study to Assess the Efficacy of Tradipitant in Relieving Symptoms of Gastroparesis

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Updated on 19 February 2024

Summary

The main purpose of this study is to see if an experimental drug, TRADIPITANT can help people with diabetic or idiopathic gastroparesis who are suffering from nausea.

Description

Who is eligible? • Patients with idiopathic or diabetic gastroparesis with moderate to severe nausea • Patients must have had nausea symptoms for at least 6 months If you participate in the study you will receive the following: Physical examinations, laboratory tests, study related medications. All procedures and medication are provided at no charge to you. How long will I be in the study? The total time in the study could be up to approximately 9 weeks. Will I be paid to be in the study? Patients will be compensated for time and travel.

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Details
Condition Nausea,Vomiting,Gastroparesis
Age 18years - 70years
Clinical Study IdentifierTX5559
Last Modified on19 February 2024

Eligibility

If you need help finding a study or have any questions, please contact us at psom-ocr@pobox.upenn.edu

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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