GEBT Telehealth Administration Usability Study
Completed · Not applicable
Conditions studied: Gastroparesis
In brief
The purpose of this study is to establish the usability of a telehealth platform for the administration of GEBT.
Key facts
- Study ID
- NCT04684992
- Run by
- Cairn Diagnostics
- People needed
- 36
- Starts
- 2020-12-11
- Expected to finish
- 2021-03-10
- Last updated by the study team
- 2021-08-24
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Males and females, greater than or equal to 18 years of age at the time of signing the consent form, from healthy and intended use population (i.e. symptomatic for gastroparesis). Women of childbearing potential must not be pregnant at the time of GEBT administration.
- Ability to eat test meal and provide breath samples
- Access to a microwave oven at home
- Internet connection and telehealth accessible device (smart phone/tablet/computer with visual and voice capability) at home
- Environment to sit comfortably and quietly at home
You may not qualify if…
- History or physical exam suggestive of systemic disease such as pathophysiologic disorders such as renal failure, chronic heart disease, chronic respiratory disease, liver disease, or malabsorption syndrome
- History of abdominal surgery except appendectomy
- Females on hormone replacement therapy other than birth control medications
- Receipt of any investigational drug within 4 weeks of the study
- Pregnancy
- Intolerance or allergy to any component of GEBT meal
- History of neurological or psychiatric disorders
Where it is running
- Cairn Diagnostics — Brentwood, Tennessee, United States
Full record on ClinicalTrials.gov
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