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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01559883
Other study ID # DE-Thrombose-NIS-2012
Secondary ID
Status Completed
Phase N/A
First received March 1, 2012
Last updated August 14, 2014
Start date February 2012
Est. completion date December 2013

Study information

Verified date November 2013
Source LEO Pharma
Contact n/a
Is FDA regulated No
Health authority Germany: Federal Institute for Drugs and Medical Devices
Study type Observational

Clinical Trial Summary

The study aims to document the flow of German patients with cancer and acute deep vein thrombosis from first visit to diagnosis and treatment, the applied diagnostic procedures, and therapy modalities.


Recruitment information / eligibility

Status Completed
Enrollment 76
Est. completion date December 2013
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patient with cancer and acute deep vein thrombosis and/or pulmonary embolism

Exclusion Criteria:

- life expectancy less that 6 months

- age less that 18 years

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Intervention

Other:
no intervention is being made
This is a Non-Interventional Study (NIS)

Locations

Country Name City State
Germany Prof. Dr. Axel Matzdorff Saarbrücken Saarland

Sponsors (1)

Lead Sponsor Collaborator
LEO Pharma

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary treatment time on low molecular weight heparin 1 year No
Secondary patient pathways data collection on patient pathway: who is the referring physician, physician who diagnoses deep vein thrombosis (DVT) 1 year No
Secondary risk factors for DVT 1 year No
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