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Self-management of Anticoagulation Treatment

U

University of Bergen

Status

Completed

Conditions

Venous Thromboembolism
Atrial Fibrillation
Artificial Heart Valve

Treatments

Other: Training

Study type

Interventional

Funder types

Other

Identifiers

NCT02864537
Lokkebo

Details and patient eligibility

About

The aim of the study was to compare self-management of anticoagulant treatment with conventional anticoagulant treatment in Norway.

Full description

Patients (n=132) on anticoagulant treatment with warfarin participated in a 21 weeks training program where they learned how to analyse International Normalised Ratio (INR) using the point-of-care instrument CoaguChek®XS and dose warfarin. The patients had to display their skills through a test before considered self-managing. They continued to measure INR weekly for two years. All INR values during the training program and self-control period were collected. In addition, the patients were told to notify if they had any complications during this period. INR values and complications two years before enrolment was collected from INR cards and/or their general practioner. The participant filled in a quality of life-questioner at enrolment and after two years of self-management.

Enrollment

130 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • On life-long oral anticoagulation therapy
  • Judged to be qualified for patient self-management anticoagulation treatment by their GP
  • Motivated to follow the training program

Exclusion criteria

  • Drug abuse
  • Liver disease

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

130 participants in 2 patient groups

Conventional treatment
No Intervention group
Description:
Conventional anticoagulation treatment Before enrolment
Self-management
Experimental group
Description:
Trained to monitor INR and dose warfarin
Treatment:
Other: Training

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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