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Self-management of Anticoagulation Treatment

U

Una Ørvim Sølvik

Status

Completed

Conditions

Long-term Oral Anticoagulant Therapy

Treatments

Other: Training

Study type

Interventional

Funder types

Other

Identifiers

NCT02371772
UBergen

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=23) on anticoagulant treatment with warfarin participated in a 27 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 28 weeks. 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. Ten INR values and complications 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 28 weeks of self-management.

Enrollment

23 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • on life-long oral anticoagulation therapy
  • Live in Bergen municipality
  • 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

23 participants in 2 patient groups

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

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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