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

Acute Aortic Dissection Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03381716
• Other study ID #: SYNH-20171207
• Status: Completed
• Phase: N/A
• First received: December 11, 2017
• Last updated: December 18, 2017
• Start date: June 19, 2002
• Est. completion date: May 29, 2016

Study information

• Verified date: December 2017
• Source: Shenyang Northern Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

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

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 ).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 884
• Est. completion date: May 29, 2016
• Est. primary completion date: May 29, 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 21 Years to 89 Years

Eligibility

Inclusion Criteria:

• acute aortic dissection

Exclusion Criteria:

• Chronic aortic dissection

Related Conditions & MeSH terms

• Acute Aortic Dissection
• Sex Role

Intervention

Drug:
• drug
Application bracket

Procedure:
• Surgery
Surgery

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Shenyang Northern Hospital

References & Publications (1)

Bossone E, LaBounty TM, Eagle KA. Acute aortic syndromes: diagnosis and management, an update. Eur Heart J. 2017 Jun 30. doi: 10.1093/eurheartj/ehx319. [Epub ahead of print] — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The outcome measure describes aortic disease-related death,aortic dissection, paraplegia, myocardial ischemia, renal insufficiency and other aortic complications.	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.	2.9years