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Prokinetic Agent
Domperidone for Gastrointestinal Disorders
Phase 3
Recruiting
Led By Mehnaz Shafi
Research Sponsored by M.D. Anderson Cancer Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Symptoms or manifestations of: a) gastroparesis; b) refractory gastroesophageal reflux disease (GERD) including persistent esophagitis, refractory heartburn, reflux-related laryngitis, and respiratory symptoms; or c) severe dyspepsia
Patients with GI disorders who have failed standard therapy
Must not have
Patients who are receiving antiarrhythmic medications with action on repolarization times (with prolongation of the QTc interval such as amiodarone, disopyramide, dofetilide, flecainide, ibutilide, quinidine, sotalol, dronedarone etc.)
Patients with a history of or active liver failure
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 30 days after completion of study treatment
Awards & highlights
No Placebo-Only Group
Pivotal Trial
Summary
This trial studies how well domperidone works in treating patients aged 16 and older with gastrointestinal disorders. Domperidone helps the stomach move food more effectively by making its muscles contract. This can reduce symptoms like pain, bloating, nausea, and vomiting.
Who is the study for?
This trial is for patients with chronic gastrointestinal disorders like gastroparesis, severe heartburn, or indigestion that haven't improved with standard treatments. They must have stable blood counts and organ function, no other causes for their symptoms after a full check-up, and agree to the study's terms. It's not open to pregnant women, those on certain heart drugs or MAO inhibitors, people allergic to domperidone, or anyone with specific heart conditions or severe liver issues.
What is being tested?
The trial is testing how effective domperidone is in treating chronic gastrointestinal disorders by seeing if it can help control symptoms such as pain, bloating, nausea and vomiting. This involves taking the medication and completing questionnaires about symptom changes.
What are the potential side effects?
Domperidone may cause side effects including dry mouth, abdominal cramps, dizziness; it might also affect heartbeat rhythm (QT interval prolongation) which could be serious. Other less common side effects include headache and trouble sleeping.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have severe stomach issues like gastroparesis, GERD, or dyspepsia.
Select...
My GI disorder hasn't improved with standard treatments.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am taking medication that affects my heart's rhythm.
Select...
I have a history of or currently have liver failure.
Select...
I have a history of serious heart conditions.
Select...
I have a tumor in my pituitary gland that releases prolactin.
Select...
I am currently taking MAO inhibitors.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline to 30 days after completion of study treatment
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline to 30 days after completion of study treatment
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Attenuation of symptoms associated with disorder(s) of gastrointestinal motility, measured by change in Gastroparesis Cardinal Symptom Index (GSCI) score from baseline
Secondary study objectives
Change in patients' self-report of symptoms
Incidence of toxicities assessed according to the Common Terminology Criteria for Adverse Events version 4.0
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Treatment (domperidone)Experimental Treatment2 Interventions
Patients receive domperidone PO TID or QID. Treatment continues in the absence of disease progression or unacceptable toxicity.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Domperidone
2011
Completed Phase 4
~401020
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for gastroparesis include prokinetic agents like domperidone and erythromycin, which stimulate stomach contractions to enhance gastric emptying. Domperidone works by blocking dopamine receptors, thereby increasing gastrointestinal motility, while erythromycin mimics the action of motilin, a hormone that stimulates gastric contractions.
For refractory cases, gastric electrical stimulation and endoscopic pyloromyotomy are used; these methods improve gastric emptying by electrically stimulating the stomach muscles or surgically modifying the pylorus. These treatments are essential for gastroparesis patients as they directly address the impaired gastric motility, reducing symptoms such as nausea and vomiting.
Oesophageal and gastric motility disorders in patients categorised as having primary anorexia nervosa.Human antroduodenal motility, pyloric closure, and domperidone.Effect of Phoneutria nigriventer spider venom on gastric emptying in rats.
Oesophageal and gastric motility disorders in patients categorised as having primary anorexia nervosa.Human antroduodenal motility, pyloric closure, and domperidone.Effect of Phoneutria nigriventer spider venom on gastric emptying in rats.
Find a Location
Who is running the clinical trial?
M.D. Anderson Cancer CenterLead Sponsor
3,065 Previous Clinical Trials
1,802,024 Total Patients Enrolled
National Cancer Institute (NCI)NIH
13,917 Previous Clinical Trials
41,014,265 Total Patients Enrolled
Mehnaz ShafiPrincipal InvestigatorM.D. Anderson Cancer Center
1 Previous Clinical Trials
284 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am taking medication that affects my heart's rhythm.I have a history of or currently have liver failure.I am not pregnant or breastfeeding, and if capable of becoming pregnant, I agree to use birth control during the study.I have a history of serious heart conditions.You are allergic to domperidone.I have agreed to take the study drug, domperidone, by signing a consent form.Your hemoglobin level is at least 8.0 grams per deciliter and not changing.I have severe stomach issues like gastroparesis, GERD, or dyspepsia.Your blood urea nitrogen (BUN) level is not too low.I have not had any GI bleeding or blockage in the last 6 weeks.I have a tumor in my pituitary gland that releases prolactin.Your liver enzyme levels are not too high.Your magnesium level is between 1.6 and 2.6 mg.Your bilirubin levels are not more than twice the normal limit.Your AST levels are not more than twice the upper limit of normal.I am currently taking MAO inhibitors.Your white blood cell count is higher than 3,000 per milliliter.Your alkaline phosphatase levels are lower than 1.5 times the normal range.My GI disorder hasn't improved with standard treatments.Your creatinine levels are within a certain range.Your potassium levels should be between 3.0 and 5.5.Your sodium, potassium, or magnesium levels in the blood are too low or too high.
Research Study Groups:
This trial has the following groups:- Group 1: Treatment (domperidone)
Awards:
This trial has 2 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Gastroparesis Patient Testimony for trial: Trial Name: NCT01696734 — Phase 3
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