Willebrand International Non-interventional Global Surveillance

LFB

Status: Completed

Conditions: Von Willebrand Disease

Study type: Observational

Funder types: Industry

Identifiers

NCT01949220

WINGS

Details and patient eligibility

About

Collect information about WILLFACT or WILFACTIN in their real life clinical use and identify the therapeutic practices in an international environment.

Full description

Non-interventional, prospective, non comparative, international, multicentre study.

Enrollment: 80 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients with inherited von Willebrand disease
• Patients treated with WILLFACT or WILFACTIN
• Patient or parent/legal representative who has provided written signed and dated informed consent before any data collection.

Exclusion criteria

• Patients who usually do not keep injection log up to date, when treated.

Trial design

80 participants in 1 patient group

Von Willebrand factor deficient patient

Description:

Inherited von Willebrand disease