Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:19 PM
Ignite Modification Date:
2025-12-24 @ 11:19 PM
NCT ID:
NCT00916656
Eligibility Criteria:
Inclusion Criteria:
* Documented congenital fibrinogen deficiency (afibrinogenemia and hypofibrinogenemia), expected to require treatment for bleeding
* Presenting with an episode of acute bleeding (either spontaneous or after trauma) not requiring surgery
* Provide informed consent
Exclusion Criteria:
* Life expectancy \< 6 months
* Bleeding disorder other than congenital fibrinogen deficiency, but including dysfibrinogenemia
* Treatment with any investigational medicinal product (IMP) in the 30 days prior to enrollment
* Treatment with any fibrinogen concentrate or other fibrinogen containing blood product in the 2 weeks prior to enrollment
* Treatment with any coagulation active drug (i.e., non-steroidal-antirheumatics, warfarin, cumarin derivates, platelet aggregation inhibitors) in 1 week prior to enrollment or as a planned or expected medication during the time period from Day 1 until 24 hours after the last FCH infusion
* Presence or history of hypersensitivity to FCH
* Presence or history of deep vein thrombosis or pulmonary embolism within 1 year prior to enrollment
* Presence or history of arterial thrombosis within 1 year prior to enrollment
* Presence or history of hypersensitivity to human plasma proteins
* Presence or history of esophageal varicose bleeding
* End stage liver disease (i.e., Child Pugh score B or C)
* Planned or expected surgery (i.e., for bleedings from aneurysm or splenic rupture)
* Pregnancy, or an intention to become pregnant during the study
* Currently breast-feeding, or with the intention of breast-feeding during the study
* Human immunodeficiency virus (HIV) positive
* Polytrauma, present or within 6 months prior to enrollment
* Suspicion of an anti-fibrinogen inhibitor as indicated by previous in-vivo recovery (IVR), if available (\< 0.5 (mg/dL)/(mg/kg))
* Previous inclusion and treatment in the prospective part of the study
* Participation in any clinical study in the 30 days prior to enrollment
Healthy Volunteers:
False
Sex:
ALL
Study:
NCT00916656
Study Brief:
Protocol Section:
NCT00916656