Clinical Trials Directory

Trials / Completed

CompletedNCT02267941

Risk Factors for Aortic Dissection in the Chinese Patients

Food and Drug Administration in China

Status
Completed
Phase
Study type
Observational
Enrollment
3,045 (actual)
Sponsor
General Hospital of Beijing PLA Military Region · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

To evaluate epidemiological features of risk factors for aortic dissection (AD) in Chinese patients.

Detailed description

Aortic dissection (AD) is a life-threatening cardiovascular disease with high mortality. Without optimal treatment, approximately 50% of patients die within one week of the onset of symptoms, and 80% die within 2 weeks. With the change of life-style and the development of diagnostic technology, the incidence and detection rate of AD were increasing in China recently. However, the cause remains unclear. Studies showed that AD were associated with some risk factors, such as hypertension, connective tissue disease, iatrogenic injury, drug, pregnancy, etc. It is reported that two thirds patients with AD had a history of hypertension; 50% patients aged \<40 years were accompanied with hereditary Marfan syndrome; 13~19% had a familial history of aortic aneurysm or dissection. These epidemiological data were obtained from Caucasian population, however, such information was not available for the Chinese population. Moreover, epidemiological investigation was absent in China, and the assessment of risk factors for AD was mainly referred to the studies from developed countries. Therefore, the aim of our study was to evaluate epidemiological features of risk factors for AD in Chinese patients using 3045 individuals from the 15 major centers in China. We anticipated that this analysis would provide helpful information preventing and controlling AD in China.

Conditions

Interventions

TypeNameDescription
OTHERobservationData were collected by a disigned form. Statistic software was used to analyze clinical data.

Timeline

Start date
2011-01-01
Primary completion
2011-01-01
Completion
2013-12-01
First posted
2014-10-20
Last updated
2014-10-20

Source: ClinicalTrials.gov record NCT02267941. Inclusion in this directory is not an endorsement.