New MRI technique could shed light on stomach disorder
NCT ID NCT04282317
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study uses MRI scans to look at the brain and upper digestive tract in people with gastroparesis and healthy volunteers. The goal is to better understand how the brain and gut interact in this condition. Researchers will compare stomach movements before and after meals. This is an observational study, not a treatment trial.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to better non-invasive imaging methods to understand and diagnose gastroparesis.
- What could go wrong
- This is a small, early-stage observational study with only 31 participants, so results may not apply widely. It does not test a treatment.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
31 people
The number who actually took part.
- Started
-
Aug 2019
- Expected to finish
-
Dec 2027
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 65 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
HEALTHY VOLUNTEERS Inclusion Criteria: • Healthy volunteers from 18 to 65 years of age Exclusion Criteria: * Contraindication to MR scanning: pregnancy, implanted gastric stimulator, neural stimulator, implanted cardiac pacemaker, auto-defibrillator, cochlear implant, ocular foreign body (e.g. metal shavings), pain pump, insulin pump or any pre-existing eye conditions. * Presence of gastroparesis symptoms, such as nausea, emesis, early satiety, effortless regurgitation, post-prandial fullness and pain, and/or postprandial epigastric pain. * Prior diagnosis of the upper GI disorders, including gastroparesis, gastric or duodenal ulcer, gastric outlet obstruction, acute or chronic pancreatitis, large hiatal or paraesophageal hernia, small intestinal bacterial overgrowth, celiac disease, Crohn's disease. * Prior systemic disorders associated with GI neuromuscular disorder listed in Appendix B. * Taking medications that can effect GI motility, including opiate, metoclopramide, dopamine agonist for Parkinson or restless leg syndrome, anticholinergics. * Prior brain or abdominal surgery (except cholecystectomy or appendectomy). * Prior diagnosis of central nervous system illness, neurological lesion, a psychiatric history, or recurrent migraines that require medication. * Uncontrolled medical problems, such as hypertension, pulmonary or airway disease, heart failure, or coronary artery disease. * Allergy to pineapple. * Presence of dysphagia. * Unable to give own informed consent. GASTROPARESIS PATIENTS Inclusion Criteria: * Patients with gastroparesis from 18 to 65 years of age. * Symptoms of gastroparesis of at least 12 weeks duration with varying degrees of nausea, emesis, early satiety, effortless regurgitation, post-prandial fullness and pain, and/or postprandial epigastric pain. * Abnormal 4-hour gastric emptying scintigraphy within the last 6 months \>60% retention at 2 hrs and/or \>10% retention at 4 hrs. Exclusion Criteria: * Contraindication to MR scanning: pregnancy, implanted gastric stimulator, neural stimulator, implanted cardiac pacemaker, auto-defibrillator, cochlear implant, ocular foreign body (e.g. metal shavings), pain pump, insulin pump or any pre-existing eye conditions. * Prior diagnosis of the upper GI disorders other than gastroparesis, including gastric or duodenal ulcer, gastric outlet obstruction, acute or chronic pancreatitis, large hiatal or paraesophageal hernia, small intestinal bacterial overgrowth, celiac disease, Crohn's disease . * Prior brain or abdominal surgery (except cholecystectomy or appendectomy). * Prior diagnosis of central nervous system illness, neurological lesion, a psychiatric history, or recurrent migraines that require medication. * Uncontrolled medical problems, such as hypertension, pulmonary or airway disease, heart failure, or coronary artery disease. * Allergy to pineapple. * Prior history of dysphagia. * Unable to give own informed consent.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Gastroparesis are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Indiana University School of Medicine
Indianapolis, Indiana, 46202, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Ultrasound could reveal when ICU tube feeding fails
- Stomach sensor may unmask hidden effects of weight-loss drugs
- A sticker-based stomach scan may replace radioactive tests for a chronic digestive disorder
- Can a stomach muscle cut tame diabetes blood sugar?
- Could a skin patch ease stomach pain in scleroderma?
- Could a botox shot in the gut ease Kids' chronic vomiting?