Hypofibrinogenemia
Information
- Disease name
- Hypofibrinogenemia
- Disease ID
- Description
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT05780125 | Completed | Phase 2 | Effectiveness of Different Fibrinogen Preparations in Restoring Clot Firmness | March 20, 2023 | February 6, 2024 |
| NCT02822599 | Completed | Phase 4 | Human Fibrinogen Concentrate in Pediatric Cardiac Surgery | June 1, 2017 | December 24, 2020 |
| NCT06434389 | Not yet recruiting | A Point-of-care Electrochemical-based Device for Rapid Detection of Fibrinogen on Type A Aortic Dissection Surgery | June 1, 2024 | November 30, 2024 | |
| NCT05634005 | Recruiting | N/A | Clinical Decision Support for Blood Transfusions to Improve Guideline Adherence | February 1, 2023 | December 2024 |
| NCT05711524 | Recruiting | Phase 4 | Transfusion of Pathogen Reduced Cryoprecipitated Fibrinogen to Expedite Product Availability in Perioperative Bleeding | April 1, 2023 | March 2025 |
| NCT03884725 | Unknown status | Phase 4 | Fibrinogen Concentrate In Children Cardiac Surgery 2 | March 1, 2019 | June 2019 |
| NCT04636268 | Withdrawn | Phase 3 | FIB Grifols Congenital Deficiency for On-demand Treatment and Surgical Prophylaxis | December 2023 | March 2025 |
| NCT00916656 | Withdrawn | Phase 3 | Fibrinogen Concentrate (Human) - Efficacy and Safety Study | October 2009 | March 2014 |
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0011900
- MedGen concept unique identifier (MedGen Concept name)
- C0553681
- MedGen unique identifier (MedGen Concept name)
- 107511