Gastroparesis Trial, Recruiting NCT04699591 Sponsor: Jose Cocjin Condition: Gastroparesis
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Gastroparesis Trial, Recruiting

NCT04699591
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 can be male or female.
  • You must be between 12 and 21 years old.
  • You have symptoms related to acid reflux (GERD) — such as ongoing inflammation of the esophagus, heartburn, throat or breathing problems — or digestive issues like nausea, vomiting, severe indigestion, or long-term constipation that have not improved with standard treatments.
  • You must have had a thorough medical evaluation to rule out other possible causes of your symptoms.
  • You (and/or your parent or guardian) must have signed a consent form confirming you understand the possible risks of the study drug, domperidone, including effects on hormone levels, movement-related side effects, breast changes, heart rhythm changes, and possible interactions with certain medications or herbal supplements.

Who may not be able to join:

  • You have a history of, or currently have, certain heart rhythm problems, such as ventricular tachycardia, ventricular fibrillation, or a condition called Torsade des Pointes (minor irregular heartbeats may not automatically disqualify you — confirm with trial site).
  • You have a significantly slow heart rate, problems with the heart's natural pacemaker, or a condition where electrical signals in the heart are blocked, or your heart's electrical timing measurement (QTc) is too long (over 450ms for males or over 470ms for females).
  • You have a significant imbalance of important minerals or chemicals in your blood (confirm with trial site).
  • You have bleeding in your digestive tract or a blockage in your digestive system.
  • You have a type of pituitary gland tumor that produces too much of the hormone prolactin.
  • You are pregnant or currently breastfeeding.
  • You have a known allergy to the study drug, domperidone.

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 28 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.

Contact this trial

Principal Investigator: Jose Cocjin, MD, Children's Mercy Hospital Kansas City

Phone: 816-302-3076

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Jose Cocjin
Registry
ClinicalTrials.gov
Start date
1 April 2013
Est. completion
1 December 2035

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Change in disease severity

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: 28 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