Gastroparesis Outcome Longitudinal Database Enrolled Numerically
Last updated on July 2021Recruitment
- Recruitment Status
- Recruiting
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Gastroparesis
- Type
- Observational
- Design
- Observational Model: Case-OnlyTime Perspective: Other
Participation Requirements
- Age
- Younger than 125 years
- Gender
- Both males and females
Description
All patients seen with the Sx of Gp and who were evaluated for diagnosis and/or treatment Including legacy patients who were seen and treated at previous locations (Mississippi, Arkansas, Tennessee) before Kentucky if they were part of a clinical research series. Numbers of patients referred or cons...
All patients seen with the Sx of Gp and who were evaluated for diagnosis and/or treatment Including legacy patients who were seen and treated at previous locations (Mississippi, Arkansas, Tennessee) before Kentucky if they were part of a clinical research series. Numbers of patients referred or consulted for Gp Sx who were Drug Refractory. Interventions: GI Neuromodulation with gastric electrical stimulation (GES); Immunotherapy with Intravenous Immunoglobulin; Pyloric therapies such as pyloroplasty, surgical or endoscopic. Data for evaluation by: Sx assessments by whatever scales used; Measures of health related quality of life; Psychological and pain assessments; Gastric emptying texts; Electrical measures; Autonomic measure; Serologic measures; Full thickness biopsies; Measures of outpatient & Emergency Room Visits; Measures of hospitalization; Placement of endoscopic or surgical tubes; Radiological and Surgical procedures; Nutritional assessments; If enrolled in any research protocols for data; Stool biome measures; Metabolic measures; Other morbidity measures; Mortality
Tracking Information
- NCT #
- NCT03876288
- Collaborators
- Not Provided
- Investigators
- Principal Investigator: Thomas Abell, MD University of Louisville