- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00523653
The Genetics of Dilated Cardiomyopathy: A Quebec-Based Study
March 17, 2008 updated by: McGill University Health Centre/Research Institute of the McGill University Health Centre
Dilated cardiomyopathy (DCM) affects about 200,000 Canadians.
Eighty percent of these cases are of unclear cause, often occuring in families.
We believe that mutations in specific already-identified genes contribute to DCM in Quebec and that certain mutations may account for a significant proportion of cases due to the well-documented "founder effect".
Two hundred patients with DCM followed in our Heart Function Clinic will be approached for one blood sample at their routine clinic visit to test this hypothesis.
The samples will be tested in the Laboratory of Cardiovascular Genetics at the Royal Victoria Hospital.
Study Overview
Study Type
Observational
Enrollment (Anticipated)
200
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Nadia S Giannetti, MD
- Phone Number: 32850 (514)934 1934
- Email: nadia.giannetti@much.mcgill.ca
Study Locations
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Quebec
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Montreal, Quebec, Canada, H3A 1A1
- Recruiting
- Royal Victoria Hospital
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Contact:
- Nadia Giannetti, MD
- Email: nadia.giannetti@muhc.mcgill.ca
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients with Dilated cardiomyopathy followed at the Heart Function Clinic and their families
Description
Inclusion Criteria:
- Followed at MUHC Heart Function Centre
- Documented EF of less than or equal to 35% and an enlarged heart with a left ventricular end-diastolic size of greater than 6 cm.
- Patient's written consent
Exclusion Criteria:
- Patients with a known underlying condition that results in a weakened and enlarged heart
- Patients unable to read and understand the consent form
- Patients who do not wish to participate
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Nadia S Giannetti, MD, McGill University Hospital Centre
- Principal Investigator: Jamie Engert, PhD, McGill University Health Centre/Research Institute of the McGill University Health Centre
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2008
Study Completion (Anticipated)
December 1, 2008
Study Registration Dates
First Submitted
August 29, 2007
First Submitted That Met QC Criteria
August 29, 2007
First Posted (Estimate)
August 31, 2007
Study Record Updates
Last Update Posted (Estimate)
March 19, 2008
Last Update Submitted That Met QC Criteria
March 17, 2008
Last Verified
March 1, 2008
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- BMB 07-004
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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