Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
500 participants
OBSERVATIONAL
2012-10-01
2025-10-01
Brief Summary
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Detailed Description
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2. Results of the physiologic measures of ACEM had the results recorded.
3. ACEM is compared to standardized gastric emptying values as the primary measure.
4. ACEM is also compared to metabolic measures of weight, height and thus BMI as a secondary measure.
5. ACEM is aloes compared with standardized gastrointestinal symptoms by a traditional patient recorded outcome as another secondary measure.
Other sites may be added if they have identical IRB and/or data sharing agreements with the University of Louisville.
Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Pregnancy
* Inability of patient or guardian to sign informed consent, if needed
* Psychiatric disorders precluding assessment and treatment of the patient's GI condition.
10 Years
80 Years
ALL
No
Sponsors
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University of Louisville
OTHER
Responsible Party
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Thomas Abell
Professor
Principal Investigators
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Thomas Abell
Role: PRINCIPAL_INVESTIGATOR
University of Louisville
Locations
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University of Louisville
Louisville, Kentucky, United States
Countries
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Central Contacts
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Facility Contacts
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Thomas Abell, MD
Role: primary
Other Identifiers
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13.0020.02
Identifier Type: -
Identifier Source: org_study_id
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