Venous Thromboembolism Clinical Trial
— DaPaROfficial title:
Safety of Dabigatran Etexilate (DE) for Treatment of Venous Thromboembolism (VTE) and Prevention of Recurrent VTE in Paediatric Patients From Birth to Less Than 2 Years of Age: a Prospective European Non-interventional Cohort Study Based on New Data Collection
The study is designed to collect and evaluate Dabigatran Etexilate (DE) safety in the context of routine anticoagulation care provided in the European Union (EU)/European Economic Area (EEA) for children under 2 years of age. The non-interventional study will be conducted in paediatric hospitals or paediatric departments of EEA member states where Venous thromboembolism (VTE) patients of the evaluated age group are treated.
Status | Recruiting |
Enrollment | 50 |
Est. completion date | October 1, 2024 |
Est. primary completion date | October 1, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A to 2 Years |
Eligibility | Inclusion criteria: - Written informed consent from parents/care givers - Children from birth to less than 2 years of age - Initiation of Dabigatran Etexilate (DE) administration: - for treatment of Venous thromboembolism (VTE) or/and - prevention of recurrent VTE due to presence of unresolved clinical VTE risk factor(s). Exclusion criteria: - Participation in any Randomised Clinical Trial or use of any investigational product - Any contraindications to DE according to the EU Summary of Product Characteristics (SmPC) |
Country | Name | City | State |
---|---|---|---|
Czechia | University Hospital Brno | Brno | |
Czechia | University Hospital Olomouc | Olomouc | |
Czechia | University Hospital Ostrava | Ostrava | |
Finland | Tampere University Hospital | Tampere | |
Germany | Charité - Universitätsmedizin Berlin | Berlin | |
Netherlands | Radboud Universitair Medisch Centrum | Nijmegen | |
Netherlands | Universitair Medisch Centrum Utrecht | Utrecht | |
Spain | Hospital Sant Joan de Déu | Barcelona | |
Spain | Hospital Materno Infantil Gregorio Marañón | Madrid | |
Sweden | Karolinska Universitetssjukhuset | Stockholm |
Lead Sponsor | Collaborator |
---|---|
Boehringer Ingelheim |
Czechia, Finland, Germany, Netherlands, Spain, Sweden,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Incidence of any bleeding events defined as Major Bleeding Events (MBE) or Non-Major Bleeding Events (Non-MBE) | Major bleeding defined as:
Fatal Bleeding, Clinically overt bleeding associated with a decrease in haemoglobin of at least 2 g/dL (20 g/L) in a 24-hour period, Bleeding that is retroperitoneal, pulmonary, intracranial, or otherwise involves the central nervous system, Bleeding that requires surgical intervention in an operating suite. Non-Major bleeding defined as: - Any overt or macroscopic evidence of bleeding that does not fulfil the criteria for major bleeding. (Criteria for differentiation of Major Bleeding Events (MBEs) and Non-MBEs by the Perinatal and Paediatric Haemostasis Subcommittee of the Scientific and Standardization Committee (SSC) of the International Society on Thrombosis and Haemostasis (ISTH).) |
up to 6 months | |
Secondary | Incidence of Adverse Events (AEs) | up to 6 months | ||
Secondary | Incidence of Serious Adverse Events (SAEs) | up to 6 months |
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