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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02306200
Other study ID # HUM00052866
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 2013
Est. completion date August 2053

Study information

Verified date May 2023
Source University of Michigan
Contact Lauren Humphrey-Stark, BS
Phone 7342324779
Email ljeany@med.umich.edu
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The goal of this project is to establish a biobank of clinical information, DNA, plasma, and aortic tissue samples from patients with cardiovascular disease as well as healthy controls.


Description:

The goal of this project is to establish a biobank of clinical information, DNA, plasma, and aortic tissue samples from patients with cardiovascular disease as well as healthy controls. The aims of the study are to collect biological specimens (blood, plasma, serum, aortic tissue) and family history; establish a biobank, establish a comprehensive database with information from consented patients, and provide researchers with high quality well annotated DNA samples with demographic and clinical information.


Recruitment information / eligibility

Status Recruiting
Enrollment 9999
Est. completion date August 2053
Est. primary completion date August 2053
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Any patient over the age of 18 who is able/willing to give informed consent - Patients <18 years of age with parental consent and assent (if assent is applicable for their age) - Diagnosis of: - aortic pathology potentially due to a known or suspected inherited condition - Idiopathic aortic aneurysm - Interesting of novel vascular pathology in the aorta or main branches - Family history of aortic or vascular disease - Other cardiovascular disease - Healthy controls with no apparent cardiovascular disease Exclusion Criteria: - Not willing or able to sign the consent

Study Design


Locations

Country Name City State
United States University of Michigan Ann Arbor Michigan

Sponsors (1)

Lead Sponsor Collaborator
University of Michigan

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Establishing a biobank of patients with Aortic Disease Establish a biobank of blood, serum, plasma, tissue, and clinical data of patients with any form of aortic disease 40 years
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