Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Philadelphia, Pennsylvania 19124


Purpose:

Gastroparesis is a digestive disorder in which motility of the stomach is either slowed or absent. The gastroparesis prevents normal digestion from occurring. The purpose of this study is to provide oral Domperidone offered under the U.S. Food and Drug Administration (FDA) expanded access program, to patients that, based on the treating doctor's assessment, could benefit from , a prokinetic effect for the relief of refractory gastroesophageal reflux disease with upper gastrointestinal (GI) symptoms, gastroparesis, and chronic constipation.


Study summary:

At the discretion of the Investigator, 10-30 mg of oral domperidone is administered QID (four times a day). The Investigator will be starting patients on 10 mg four times a day for 2 weeks, then increase to 20 mg four times a day for 2 weeks. The participant will be evaluated at each time point. If the participant still is not having relief of symptoms the investigator may increase their dose to 30mg four times a day.


Criteria:

Inclusion Criteria: 1. Male or female 2. Age 18 and older 3. Symptoms or manifestations secondary to GERD (e.g., persistent esophagitis, heartburn, upper airway signs or symptoms or respiratory symptoms), gastrointestinal motility disorders such as nausea, vomiting, severe dyspepsia or severe chronic constipation refractory to standard therapy. 4. Patients must have a comprehensive evaluation (physical exam and also may include EGD, gastric emptying study, as clinically necessary) to eliminate other causes of their symptoms. 5. Patient has signed informed consent for the administration of domperidone that informs the patient of potential adverse events including: - increased prolactin levels - extrapyramidal side-effects - breast changes - cardiac arrhythmias including QT prolongation and death Exclusion Criteria: History of, or current, arrhythmias including ventricular tachycardia, ventricular fibrillation and Torsade des Pointes. Patients with minor forms of ectopy (PACs) are not necessarily excluded. 1. Clinically significant bradycardia, sinus node dysfunction, or heart block. Prolonged QTc (QTc> 450 milliseconds for males, QTc>470 milliseconds for females). 2. Clinically significant electrolyte disorders. 3. Gastrointestinal hemorrhage or obstruction 4. Presence of a prolactinoma (prolactin-releasing pituitary tumor). 5. Pregnant or breast feeding female 6. Known allergy to domperidone


NCT ID:

NCT02494687


Primary Contact:

Raman Battish, MD
Phone: 215-537-7400
Email: Raman.Battish@ctca-hope.com


Backup Contact:

Email: Jack.Medendorp@ctca-hope.com
Jack Medendorp
Phone: 215-537-3160


Location Contact:

Philadelphia, Pennsylvania 19124
United States

Raman Battish, MD
Phone: 215-537-7400
Email: Raman.Battish@ctca-hope.com

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 18, 2019

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.