Response to Medication Registry

Status Completed

Clinical Trial Summary

To create a registry/database of patients who either have taken drugs that treat cardiovascular conditions or that have presented with cardiovascular symptoms that may be related to medication.

Clinical Trial Description

To create a registry/database of patients who either have taken drugs that treat cardiovascular conditions or that have presented with cardiovascular symptoms that may be related to medication. Potential enrollees are those receiving (presently or in the past) the medicine(s) of interest. Subjects will be identified from computerized Intermountain Healthcare records. Patients receiving a drug of interest, both with and without an ADE will be enrolled in approximately equal numbers. Outpatients will be contacted by mail and invited to participate. Interested subjects will be instructed to return the enclosed response card with their intent indicated. The registry coordinator will contact interested subjects and the project will be explained. Willing participants will be enrolled either in person or via mail with the assistance of the project coordinator. Persons presenting in person for enrollment will be given the choice of venipuncture or buccal swab for sample collection for DNA extraction. In all cases informed consent will be obtained before collecting samples. ;

Study Design

Related Conditions & MeSH terms

Adverse Drug Events
Drug-Related Side Effects and Adverse Reactions

Clinical Trial Details

NCT number	NCT02593916
Study type	Observational [Patient Registry]
Source	Intermountain Health Care, Inc.
Contact
Status	Completed
Phase
Start date	March 2007
Completion date	December 2018

View Details

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