🔬 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
This study tests the effects of an investigational antipsychotic drug (call...
Status
Completed
Location
Multiple Locations
Start Date
2010-03-16
Trial ID
NCT01074294
Treatments Being Tested
The general goal of the present proposal, Progetto MOSAICO, is the identifi...
Status
Completed
Location
IRCCS E. Medea
Start Date
2018-01-02
Trial ID
NCT04769011
This study aims to validate that PLGF is a biomarker of cerebral lesions an...
Status
Recruiting
Location
UH ROUEN
Start Date
2017-01-27
Trial ID
NCT03371641
Obstructive sleep apnea (OSA) is part of the sleep-disordered breathing spe...
Status
Recruiting
Location
Hôpital Femme-Mère-Enfant : Service d'épileptologie clinique, des troubles du sommeil et de neurologie fonctionnelle de l'enfant
Start Date
2026-03-26
Trial ID
NCT07273019
With the advent of new treatments for ASI, new phenotypes are emerging. The...
Status
Recruiting
Location
Pediatric Rehabilitation Service - L'Escale Mother and Child Hospital
Start Date
2024-07-24
Trial ID
NCT06321965
The survival rate of children with cancer has improved significantly in rec...
Status
Recruiting
Location
Gustave Roussy
Start Date
2014-10-01
Trial ID
NCT03609112
Treatments Being Tested
The most common neuropsychiatric disorder in early childhood is attention d...
Status
Completed
Location
Assiut University Hospital
Start Date
2019-02-15
Trial ID
NCT03806946
Multiple forms of Omega-3 Fatty acids have been used to investigate the rol...
Status
Terminated
Location
Maimonides Medical Center
Start Date
2009-12
Trial ID
NCT01778647
Treatments Being Tested
To analyze heterogeneity in ADHD experts in last decade advised to look bey...
Status
Completed
Location
Alessandra Carta
Start Date
2017-01-18
Trial ID
NCT04326543
Treatments Being Tested
FOXP1 syndrome is a rare genetic disorder with a variable phenotype, charac...
Status
Completed
Location
Hôpital Necker-Enfants Malades
Start Date
2024-01-19
Trial ID
NCT06211673
Treatments Being Tested