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Clinical Trials/NCT03381716
NCT03381716
Completed
Not Applicable

Correlation Between Sex and Prognosis of Acute Aortic Dissection in the Chinese Population

Shenyang Northern Hospital0 sites884 target enrollmentJune 19, 2002

Overview

Phase
Not Applicable
Intervention
Surgery
Conditions
Acute Aortic Dissection
Sponsor
Shenyang Northern Hospital
Enrollment
884
Primary Endpoint
The outcome measure describes aortic disease-related death,aortic dissection, paraplegia, myocardial ischemia, renal insufficiency and other aortic complications.
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The study evaluated the prevalence, presentation, management, and prognosis of coronary heart disease differ according to sex.

Detailed Description

The study included 884 patients enrolled in our institute between June 2002 and May 2016. Considering psychosocial factors, treatments, and the outcomes in men versus those in women with acute aortic dissection, explored the association of sex with psychosocial characteristics and mortality risk. Of 884 patients, 211 (23.9%) were women. The median duration of follow-up was 2.9 years (25th -75th percentiles: 1-4 years ).

Registry
clinicaltrials.gov
Start Date
June 19, 2002
End Date
May 29, 2016
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Shenyang Northern Hospital
Responsible Party
Principal Investigator
Principal Investigator

Han Yaling, MD

Correlation between sex and prognosis of acute aortic dissection in the Chinese population

Shenyang Northern Hospital

Eligibility Criteria

Inclusion Criteria

  • acute aortic dissection

Exclusion Criteria

  • Chronic aortic dissection

Arms & Interventions

female

Drug:Beta-blocker,Angiotensin II receptor blocker,Angiotensin-converting enzyme,Calcium-channel blocker,Aspirin,Statin

Intervention: Surgery

male

Drug:Beta-blocker,Angiotensin II receptor blocker,Angiotensin-converting enzyme,Calcium-channel blocker,Aspirin,Statin

Intervention: drug

male

Drug:Beta-blocker,Angiotensin II receptor blocker,Angiotensin-converting enzyme,Calcium-channel blocker,Aspirin,Statin

Intervention: Surgery

female

Drug:Beta-blocker,Angiotensin II receptor blocker,Angiotensin-converting enzyme,Calcium-channel blocker,Aspirin,Statin

Intervention: drug

Outcomes

Primary Outcomes

The outcome measure describes aortic disease-related death,aortic dissection, paraplegia, myocardial ischemia, renal insufficiency and other aortic complications.

Time Frame: 2.9years

The study's primary endpoint during the follow up was the composite of aortic disease-related death, aortic dissection, paraplegia, myocardial ischemia, renal insufficiency and other aortic complications during follow-up.

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