Study on Genetically Affected Sporadic Thoracic Aortic Aneurysm and Dissection
GenSTAND
1 other identifier
observational
450
1 country
1
Brief Summary
Mortality of thoracic aortic aneurysm and dissection (TAAD) remains high because of the huge blood lost from the aorta. Questions about the potentially genetic effects on sporadic TAAD are raised by researchers to explore the possible mechanisms leading to sporadic TAAD and to establish new clinical approaches to prevent TAAD-caused adverse clinical outcomes. This study is intended to collect the gene information in sporadic TAAD patients and to explore the relationship between genetic variation and the incidence of sporadic TAAD for further study.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Aug 2014
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 1, 2014
CompletedFirst Submitted
Initial submission to the registry
July 27, 2016
CompletedFirst Posted
Study publicly available on registry
August 2, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2020
CompletedApril 13, 2021
April 1, 2021
4.4 years
July 27, 2016
April 11, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Numbers of patients having thoracic aortic aneurysm and/or dissection are recorded. Diagnosis are confirmed by imaging analysis (CTA and/or Ultrasound) or by doctors during the operations.
Arterial dissection actually happened
6 months
Study Arms (1)
thoracic aortic aneurysm and dissection
Patients with thoracic aortic aneurysm and/or dissection are recruited in the study.
Eligibility Criteria
Patients with thoracic aortic aneurysm and dissection.
You may qualify if:
- Patients with thoracic aortic aneurysm and dissection not due to trauma
You may not qualify if:
- Inability of the patient, parent or guardian to give consent
- Unwillingness to provide a blood specimen or participate in the study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Wuhan Asia Heart Hospitallead
- Fu Wai Hospital, Beijing, Chinacollaborator
Study Sites (1)
Wuhan Asia Heart Hospital
Wuhan, Hubei, 430022, China
Biospecimen
Peripheral whole blood is obtained from patients. Serum, blood cell and DNA are separated and stored for further study.
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Xuan Zheng, MD, PhD
Wuhan Asia Heart Hospital
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- vice director of laboratory of molecular cardiology
Study Record Dates
First Submitted
July 27, 2016
First Posted
August 2, 2016
Study Start
August 1, 2014
Primary Completion
January 1, 2019
Study Completion
January 1, 2020
Last Updated
April 13, 2021
Record last verified: 2021-04