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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02214043
Other study ID # APEINCP
Secondary ID
Status Completed
Phase N/A
First received February 3, 2014
Last updated January 28, 2018
Start date January 2012
Est. completion date December 2017

Study information

Verified date July 2016
Source Chinese Pulmonary Vascular Disease Research Group
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

There are no special clinical characteristics of acute pulmonary embolism in Chinese population.


Recruitment information / eligibility

Status Completed
Enrollment 600
Est. completion date December 2017
Est. primary completion date December 2017
Accepts healthy volunteers No
Gender All
Age group 15 Years to 85 Years
Eligibility Inclusion Criteria:

- the symptomatic acute PE confirmed by objective examination

Exclusion Criteria:

- congestive heart failure

- chronic obstructive pulmonary disease;

- a prior documented episode of PE or DVT

- renal dysfunction;

- a life expectancy of less than 6 months

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Center of pumonary vascular diseases Beijing

Sponsors (1)

Lead Sponsor Collaborator
Chinese Pulmonary Vascular Disease Research Group

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The primary end point of the present study was symptomatic, objectively confirmed recurrent fatal or nonfatal VTE. 60 months
Secondary The second end point was death (all cause death and PE-related death). If the participant died, the relatives need provided the written medical record on the death. 60 months
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