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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01587053
Other study ID # 8745
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date April 2012
Est. completion date February 2017

Study information

Verified date November 2020
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to measure the INR (International Normalized Ratio) time percentage in the target zone (TTR: time in therapeutic range) of children benefiting from the AVK therapeutic education program.


Recruitment information / eligibility

Status Terminated
Enrollment 57
Est. completion date February 2017
Est. primary completion date February 2017
Accepts healthy volunteers No
Gender All
Age group N/A to 18 Years
Eligibility Inclusion Criteria: - age from 0 to 18 years - AVK prescription - to accept participating to AVK therapeutic education program - informed consent form of parents or legal person Exclusion Criteria: - parents or legal person refusal to enter in the AVK therapeutic education

Study Design


Intervention

Other:
therapeutic education program


Locations

Country Name City State
France Pediatric and Congenital Cardiology and Pulmonology Department, Arnaud De Villeneuve University Hospital Montpellier

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

References & Publications (1)

Abassi H, Bajolle F, Werner O, Auer A, Marquina A, Mura T, Lavastre K, Guillaumont S, Manna F, Auquier P, Bonnet D, Amedro P. Health-related quality of life correlates with time in therapeutic range in children on anticoagulants with International Normali — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary INR (International Normalized Ratio) time percentage in the target zone (TTR: time in therapeutic range) up to 1 year
Secondary Quality of life questionnaire 2 years