- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02433990
Risk Factors for Acquired Cardiovascular Disease in Adults With Congenital Heart Disease
September 17, 2019 updated by: Susan Fernandes, Stanford University
This research study is to determine the risk factors for acquired heart disease, in adults with congenital heart disease.
This knowledge is important to develop and target ways to prevent or delay the onset of acquired heart disease in adults with congenital heart disease.
Study Overview
Status
Completed
Conditions
Detailed Description
Advances in surgical and clinical management of patients with congenital heart disease has made survival to adulthood an expectation.
Today there are more than 1 million adult survivors of congenital heart disease, but increasing age brings additional concerns for this patient population.
Although the literature remains scarce, existing evidence suggests that inactivity, obesity, diabetes, cancer, and acquired cardiovascular disease may be at least as prevalent in patients with congenital heart disease, if not more so, than in an age-matched general population.
Acquired cardiovascular disease is likely to impact substantially on long-term survival and quality of life in these patients with palliated and already fragile hearts.
This research study is to determine the risk factors for acquired heart disease, in adults with congenital heart disease.
This knowledge is important to develop and target ways to prevent or delay the onset of acquired heart disease in adults with congenital heart disease.
Study Type
Observational
Enrollment (Actual)
178
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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California
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Stanford, California, United States, 940304
- Stanford Hospital and Clinics
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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
Adults with Moderate or Complex Congenital Heart Disease
Description
Inclusion Criteria:
- Male or Female over 18 years of age
- Moderate or Complex Congenital Heart Disease
- Willingness to Consent
Exclusion Criteria:
- Pregnancy
- Surgery within 6 months
- Unrepaired cyanotic heart disease
- Patients with Eisenmenger Syndrome physiology
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
Cohorts and Interventions
Group / Cohort |
|---|
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Adult Congenital Heart Disease
18 years and older with congenital heart disease
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Risk factors for acquired cardiovascular disease in adults with congenital heart disease
Time Frame: 2 years
|
2 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Susan Fernandes, PA-C, LP.D., Stanford Hospital
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 (Actual)
April 1, 2014
Primary Completion (Actual)
April 24, 2018
Study Completion (Actual)
August 24, 2019
Study Registration Dates
First Submitted
May 13, 2014
First Submitted That Met QC Criteria
April 29, 2015
First Posted (Estimate)
May 5, 2015
Study Record Updates
Last Update Posted (Actual)
September 18, 2019
Last Update Submitted That Met QC Criteria
September 17, 2019
Last Verified
September 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB-28847
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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