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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02895971
Other study ID # EPIGETBO III (RB 12.157)
Secondary ID
Status Completed
Phase N/A
First received August 29, 2016
Last updated July 3, 2017
Start date March 4, 2013
Est. completion date June 30, 2017

Study information

Verified date July 2017
Source University Hospital, Brest
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study estimate VTE incidence. Investigators prospectively record all cases of symptomatic pulmonary embolism (PE) and deep vein thrombosis (DVT) of the lower limbs diagnosed between March 1, 2013 and February 28, 2014 in hospitals and in the community.


Recruitment information / eligibility

Status Completed
Enrollment 1416
Est. completion date June 30, 2017
Est. primary completion date June 30, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- symptomatic pulmonary embolism (PE) and deep vein thrombosis (DVT) diagnosis confirmed

- Patient living in Brest area from time of diagnosis

Exclusion Criteria:

- invalid diagnosis

- asymptomatic event

- Main residence patient out of Brest area.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France CHRU de Brest Brest

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Brest

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Gathering information about potential factors predisposing Thromboembolic disease and treatments undertaken. After two years, all medication given to the patient to treat his initial VTE will be recorded, as well as the ongoing of thromboembolic disease two years after VTE
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