RECRUITING

HR-EGG in Medically Refractory Gastroparesis

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this observational study is to utilize a novel high resolution electrogastrography device to gauge if identification of gastric dysarrythmias can reliably identify patients that will respond to or will require definitive pyloric interventions such as a G-POEM procedure in patients with medically refractory gastroparesis Aims: 1. Assess for the presence of gastric dysarrythmias in lung transplantation population as compared to alternative etiologies of gastroparesis 2. Assess if presence or absence of gastric dysarrythmias is predictive of response or need of Gastric -per-oral endoscopic myotomy 3. Assess alterations in gastric dysarrthmias following pyloric interventions including G-POEM. Patients will undergo two surface body surface gastric mapping via the HR-EGG before and after undergoing a gastric per oral endoscopic myotomy as standard clinical care for the treatment of medically refractory gastroparesis

Official Title

High Resolution Electrogastrography (HR-EGG) Assessment in Medically Refractory Gastroparesis

Quick Facts

Study Start:2022-12-01
Study Completion:2025-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05789511

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adult patients (age \>17 years old) with medically refractory gastroparesis
  1. * Females who are pregnant or lactating (self-reported)
  2. * History of skin allergies to skin adhesives or hydrogels
  3. * History of extreme sensitivity to cosmetics or lotions
  4. * Fragile skin vulnerable to skin tears
  5. * Damaged epigastric skin (open wounds, rash, inflammation)
  6. * Patients unable to remain in a relaxed reclined position for the test duration
  7. * BMI \> 35 obtained via chart review

Contacts and Locations

Study Contact

Alexander J Podboy, MD
CONTACT
4349242620
JFV6DE@virginia.edu
Joanna Faulconer
CONTACT
4349242620

Study Locations (Sites)

Baylor College of Medicine
Houston, Texas, 77030
United States
University of Virginia
Charlottesville, Virginia, 22905
United States

Collaborators and Investigators

Sponsor: University of Virginia

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-12-01
Study Completion Date2025-06

Study Record Updates

Study Start Date2022-12-01
Study Completion Date2025-06

Terms related to this study

Keywords Provided by Researchers

  • Gastroparesis
  • Post- Lung Transplant

Additional Relevant MeSH Terms

  • Gastroparesis
  • Lung Transplant; Complications