🔬 Current Disease Focus:
Task Progress: 0%
👥 Active Problem Solvers
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🌍 Experts collaborating globally
⚡ Current Task Assignment
🧬 Genetic Analysis
🔄 Matching experts to specific tasks
📊 Resource Allocation by Research Phase:
📚 Data Analysis
🧪 Experimental Design
🔬 Clinical Trials
💊 Treatment Development
Congenital deficiency of factor XIII (FXIII) is an extremely rare inherited...
Status
Completed
Location
Study Site
Start Date
2009-08
Trial ID
NCT00885742
Treatments Being Tested
Many patients with Scleroderma (Systemic sclerosis) experience damage to bl...
Status
Unknown
Location
Royal Free London NHS Foundation Trust
Start Date
2015-09
Trial ID
NCT02551042
Treatments Being Tested
Congenital deficiency of Factor XIII is an extremely rare hereditary disord...
Status
Completed
Location
Study Site
Start Date
2009-05
Trial ID
NCT00883090
Treatments Being Tested
Congenital deficiency of factor XIII is an extremely rare inherited disorde...
Status
Completed
Location
Study Site
Start Date
2009-09
Trial ID
NCT00945906
Treatments Being Tested
Congenital deficiency of Factor XIII is a rare but potentially life threate...
Status
Completed
Location
Children's Hospital of Orange Co.
Start Date
2000-01
Trial ID
NCT00640289
Treatments Being Tested
Severe traumatized patients (ISS \> 15) admitted to emergency department (E...
Status
Terminated
Location
Medical University Innsbruck / Department for Anesthesia and Intensive Care Medicine
Start Date
2012-03
Trial ID
NCT01545635