Gastroparesis Trial, Recruiting NCT03603730 Sponsor: Massachusetts General Hospital Condition: Gastroparesis
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Gastroparesis Trial, Recruiting

NCT03603730
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You are a male or female volunteer between 18 and 65 years old.
  • If you are a healthy volunteer, you must be able to lie in an MRI scanner for up to 2 hours.
  • If you have been diagnosed with Functional Dyspepsia, your diagnosis must meet specific Rome III guidelines for either the PDS or EPS subtypes (confirm with trial site).
  • If you have Gastroparesis, you must have had symptoms such as nausea, vomiting, feeling full quickly, and/or bloating after eating for at least 12 weeks total (not necessarily all at once).
  • If you have Gastroparesis, your condition must have no known underlying cause (idiopathic), and you must have had an abnormal stomach-emptying scan result within the last 6 months using a specific test (confirm with trial site for exact details).
  • If you have Functional Dyspepsia or Gastroparesis, your medications for the condition must have been stable for at least one month before and during the study.
  • You must be willing to avoid alcohol, nicotine, and caffeine for 24 hours before each study session.

Who may not be able to join:

  • You have had surgery on your stomach or esophagus (food pipe).
  • You have used alternative therapies such as acupuncture or hypnosis within two weeks before or during the study.
  • You use illegal drugs or opioid medications.
  • You have a history of irregular heartbeat (arrhythmia).
  • You have an implanted pacemaker.
  • You have epilepsy or have ever had a seizure.
  • If you have Gastroparesis, you are unable to complete the required stomach-emptying scan, including if you are allergic to eggs.
  • You are pregnant, breastfeeding, or planning to become pregnant.
  • You are unable to give your own informed consent to take part.
  • Your BMI is over 32 or you weigh more than 235 lbs, due to the limits of the MRI equipment.
  • You have a history of head trauma.
  • You have any metal implants in your body, such as braces or permanent dental retainers.
  • You have tattoos with metallic ink on the upper part of your body (above the nipple line).
  • You have surgical aneurysm clips, a prosthetic heart valve, a neurostimulator, implanted pumps, cochlear implants, or metal rods, plates, or screws in your body.
  • You have had recent surgery (confirm with trial site for timing details).
  • You have an IUD (intrauterine device).
  • You use a hearing aid or dentures that may interfere with the MRI scan.
  • You have had a metal injury to your eyes.
  • You have Meniere's Disease (an inner ear condition).
  • You use medicated skin patches, such as nicotine patches, motion sickness patches, or hormonal birth control patches.
  • You experience claustrophobia (fear of enclosed spaces).

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 2 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
30 November 2018
Est. completion
30 June 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Neuroimaging

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 2 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov