Purpose

Patients seen who had autonomic and enteric profiling (Adrenergic, Cholinergic, Enteric Measures/Mapping=ACEM_ from 2012-2019 at the University of Louisville.

Condition

Eligibility

Eligible Ages
Between 10 Years and 80 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients with the symptoms suggestive of autonomic and/or enteric disorders.

Exclusion Criteria

  • Anatomic obstruction of the GI tract - Pregnancy - Inability of patient or guardian to sign informed consent, if needed - Psychiatric disorders precluding assessment and treatment of the patient's GI condition.

Study Design

Phase
Study Type
Observational
Observational Model
Case-Only
Time Perspective
Prospective

Recruiting Locations

University of Louisville
Louisville, Kentucky 40202
Contact:
Thomas Abell, MD

More Details

Status
Recruiting
Sponsor
University of Louisville

Study Contact

Thomas L Abell
(502)852-6991
thomas.abell@louisville.edu

Detailed Description

1. Patients seen who had autonomic and enteric profiling (Adrenergic Cholinergic Enteric Measures/Mapping=ACEM) from 2012-2019 at the U of Louisville. 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.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.