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A Single-center Trial of Patients With Aortic Dissection in the Chinese XinJiang Province

X

Xiang Ma

Status

Unknown

Conditions

Aortic Dissection

Study type

Observational

Funder types

Other

Identifiers

NCT02378103
IACUC-20140214090

Details and patient eligibility

About

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

Full description

The epidemiological features of risk factors for aortic dissection (AD) in China were obtained from developed population in east of China, however, such information was not available for the remote population. Moreover, people in the western region have significant difference with developed population in lifestyle, diet, ethnic and so on. Therefore, the aim of our study was to evaluate epidemiological features of risk factors for AD in Chinese remote patients. We anticipated that this analysis would provide helpful information preventing and controlling AD in Chinese XinJiang Province.

Enrollment

100 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Clinical diagnosis of aortic dissection
  2. ≥18 years old
  3. good compliance with the instructions and cooperate with follow-up voluntarily signed the informed consent form

Exclusion criteria

  1. pregnant or lactating female
  2. bad compliance with the instructions and follow-up
  3. estimated remaining life is less than 12 months
  4. Aortic aneurysm、Acute Myocardial infarction、Acute Cerebral accident

Trial design

100 participants in 2 patient groups

Case
Description:
Diagnosis of aortic dissection was based on history and physical examination, and confirmed by imaging, visualization at surgery, and/or postmortem examination. Simple aortic aneurysm and pseudoaneurysm were excluded. Simple aortic aneurysm and pseudoaneurysm were excluded. Surgical and endovascular treatments were the main interventions and performed in the case group.
Control
Description:
As the control group, patients without AD were obtained from the hospitalized patients in the same period.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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