Observational Registry of the Treatment of Glanzmann's Thrombasthenia

CompletedOBSERVATIONAL
Enrollment

218

Participants

Timeline

Start Date

January 31, 2004

Primary Completion Date

October 31, 2011

Study Completion Date

October 31, 2011

Conditions
Congenital Bleeding DisorderGlanzmann's Disease
Interventions
DRUG

activated recombinant human factor VII

A prospective, observational multi-national registry collecting data and evaluating the efficacy and safety of rFVIIa in patients with GT with past or present refractoriness to platelet transfusions. The registry will also collect data from a broader range of GT patients treated with systemic haemostatic treatment (with or without antifibrinolytic drugs or other agents) used in the clinics. Data collection will continue for a maximum of six years. Baseline data as well as data obtained during either bleeding episodes or invasive procedures/surgeries will be recorded in the registry.

Trial Locations (15)

1025

Budapest

1070

Brussels

1407

Sofia

16035

Algiers

28033

Madrid

55127

Mainz

92932

Paris La Défense Cedex

08540

Novo Nordisk Clinical Trial Call Center, Princeton

A-1010

Vienna

00144

Rome

Unknown

Alphen aan den Rijn

Karachi

202 15

Malmo

CH-8050

Zurich

RH11 9RT

Crawley

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Novo Nordisk A/S

INDUSTRY