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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01392040
Other study ID # MIV_AI_10_001
Secondary ID
Status Completed
Phase N/A
First received July 11, 2011
Last updated January 16, 2013
Start date November 2010
Est. completion date January 2013

Study information

Verified date January 2013
Source University Of Perugia
Contact n/a
Is FDA regulated No
Health authority Italy: Ethics Committee
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine whether the new algorithm is safety and effective in proposing the dosage and the timing of oral anticoagulant therapy.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date January 2013
Est. primary completion date August 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- to take oral anticoagulant therapy for at least 2 years

- to be in stable conditions for at last 3 months

Exclusion Criteria:

- patients who need to perform surgery

- patients who interrupt therapy

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Italy Hospital of Macerata Macerata

Sponsors (1)

Lead Sponsor Collaborator
University Of Perugia

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time spent in therapeutic range of INR by the patients 6 months Yes
Secondary Thrombotic and bleeding events 6 months Yes