Bumetanide
DrugAdministration by oral route in 2 times (in the morning and evening) of 0.5 mg by taking (= 1 mg by 24 hours)
NCT Number: NCT01078714
The purpose of this study is to determine if a treatment by bumetanide presents an efficiency at the level of the neuronal maturation in the autism
Looking for future studies?
Notify Me3 year–10 year
All sexes
Interventional
Phase 3
Lemonnier, Brest, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Administration by oral route in 2 times (in the morning and evening) of 0.5 mg by taking (= 1 mg by 24 hours)
Time frame: day 0 to day 90
Time frame: day 0 to day 90
Time frame: day 0 to day 90
Time frame: day 0 to day 90
University Hospital, Brest
Other
Study of the Efficiency of a Treatment by Bumetanide in a Population of Autistic Children
Acronym: BUMEA
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06875843
Animal Communication, Autism
Nashville, Tennessee, United States
View Trial DetailsNCT07277101
Autism Spectrum Disorder, Autistic Disorder
Shanghai, China
View Trial DetailsNCT01031407
Adult, Asperger Syndrome
Bethesda, Maryland, United States
View Trial DetailsNCT07720427
Autism Spectrum Disorder, Autistic Disorder
Newark, Delaware, United States
View Trial Details