Domperidone and the Risk of Serious Adverse Events

CompletedOBSERVATIONAL
Enrollment

15,000

Participants

Timeline

Start Date

January 1, 2008

Primary Completion Date

September 30, 2024

Study Completion Date

October 30, 2024

Conditions
Chronic Kidney Disease (CKD)
Interventions
DRUG

Domperidone (drug)

The primary exposure of interest will be oral domperidone at a dose of 30 mg or more per day, which represents the median dose found in high-throughput computing analyses. For the primary comparison, oral domperidone at doses below 30 mg per day will be chosen to reduce the influence of indication bias.

Trial Locations (1)

Unknown

London Health Sciences Centre Research Institute, London

All Listed Sponsors
collaborator

Canadian Institutes of Health Research (CIHR)

OTHER_GOV

lead

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

OTHER

NCT07098078 - Domperidone and the Risk of Serious Adverse Events | Biotech Hunter | Biotech Hunter