NCT02378103

Brief Summary

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

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Feb 2015

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2015

Completed
13 days until next milestone

First Submitted

Initial submission to the registry

February 14, 2015

Completed
18 days until next milestone

First Posted

Study publicly available on registry

March 4, 2015

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2016

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2016

Completed
Last Updated

February 4, 2016

Status Verified

February 1, 2016

Enrollment Period

1.1 years

First QC Date

February 14, 2015

Last Update Submit

February 3, 2016

Conditions

Keywords

Aortic DissectionChinese XinJiang Province

Outcome Measures

Primary Outcomes (1)

  • Participants with related events for aortic dissection in Chinese XinJiang population

    1 year

Study Arms (2)

Case

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

As the control group, patients without AD were obtained from the hospitalized patients in the same period.

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Between March, 2015 and March, 2016, we aim to collect 100 patients with AD as the case group. As the control group, 100 patients without AD were obtained from the hospitalized patients in the same period.

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Aortic Dissection

Condition Hierarchy (Ancestors)

Dissection, Blood VesselAneurysmVascular DiseasesCardiovascular DiseasesAcute Aortic SyndromeAortic Diseases

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
A Single-center Trial of Patients with Aortic Dissection in the Chinese XinJiang Province

Study Record Dates

First Submitted

February 14, 2015

First Posted

March 4, 2015

Study Start

February 1, 2015

Primary Completion

March 1, 2016

Study Completion

August 1, 2016

Last Updated

February 4, 2016

Record last verified: 2016-02