🔬 Current Disease Focus:
Task Progress: 0%
👥 Active Problem Solvers
0
🌍 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
Fabry disease is genetic X linked disease, with annual incidence of 1 in 10...
Status
Unknown
Location
CHU Angers
Start Date
2020-02-03
Trial ID
NCT03869554
Treatments Being Tested
The main aim of this study is early detection of FD using real-world data f...
Status
Completed
Location
Universitätsklinikum Erlangen Kinder- und Jugendklinik
Start Date
2023-11-30
Trial ID
NCT05106764
Treatments Being Tested
FD is pan-ethnic. Its reported annual incidence of 1 in 100,000 may underes...
Status
Completed
Location
CHU de Bicêtre, UNSIV (neurovascular stroke unit)
Start Date
2018-03-12
Trial ID
NCT03230149
Treatments Being Tested
Single centre, prospective pilot study examining the relevance to screen fo...
Status
Terminated
Location
Uh Montpellier
Start Date
2019-03-25
Trial ID
NCT03886714
Treatments Being Tested
The goal of this National Registry is to is to collect information from pat...
Status
Recruiting
Location
Zoe Plummer
Start Date
2009-11-06
Trial ID
NCT06065852
This research project will serve on the enhancement of early detection, dia...
Status
Unknown
Location
University Hospital of Santiago de Compostela
Start Date
2021-01-01
Trial ID
NCT04847713
Treatments Being Tested
The goal of this clinical trial is to optimise and facilitate screening for...
Status
Not Yet Recruiting
Location
Groupe Hospitalier Diaconesses Croix Saint-Simon
Start Date
2025-05
Trial ID
NCT06869499
Treatments Being Tested
Fabry disease is a rare genetic disease characterized by an enzyme deficien...
Status
Completed
Location
Service de Néphrologie - Hôpital Pasteur
Start Date
2011-06
Trial ID
NCT01374997
Treatments Being Tested
The purpose of this research is to collect biological samples (urine) to de...
Status
Unknown
Location
Lysosomal & Rare Disorders Research & Treatment Center
Start Date
2023-09-14
Trial ID
NCT06065605
The purpose of this study is to determine the prevalence of Fabry mutations...
Status
Completed
Location
AZ Imelda
Start Date
2009-07
Trial ID
NCT01198899
Treatments Being Tested