Actively Recruiting

Age: 10Years - 80Years
All Genders
ID04013282

Adrenergic Cholinergic Enteric Measures/Mapping Observational Study on Obesity and Nerve Function

Led by University of Louisville · Updated on 2025-01-10

500

Participants Needed

1

Research Sites

678 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research focuses on patients who underwent autonomic and enteric profiling called Adrenergic Cholinergic Enteric Measures/Mapping (ACEM) at the University of Louisville between 2012 and 2019. The study aims to evaluate ACEM's results by comparing them to standardized gastric emptying values as the primary measurement. Additionally, ACEM findings are compared with metabolic measures such as weight, height, and body mass index (BMI), as well as traditional patient-reported gastrointestinal symptoms as secondary measures. The study uses existing data from patients who had ACEM testing performed, with no new interventions or treatments described. While the primary focus is on the physiological and metabolic assessments, the study may include other sites if they have appropriate data sharing agreements with the University of Louisville. There are no specific treatment groups or dosing schedules involved. Participants' involvement centers around their recorded clinical and physiological data, including autonomic and enteric profiles, gastric emptying values, and metabolic information like BMI. The primary outcome measured is body mass index tracked over 10 years. Gastrointestinal symptoms reported by patients are also evaluated. This study uses retrospective data and does not describe active monitoring or follow-up visits.

CONDITIONS

Official Title

Adrenergic Cholinergic Enteric Measures/Mapping

Who Can Participate

Age: 10Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with the symptoms suggestive of autonomic and/or enteric disorders.
Not Eligible

You will not qualify if you...

  • 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.

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

University of Louisville

Louisville, Kentucky, United States, 40202

Actively Recruiting

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Research Team

T

Thomas L Abell

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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