Autism drug trial pulled before it even started
NCT ID NCT02947880
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study planned to test the drug bumetanide in children aged 5 to 17 with autism of known cause. The goal was to see if it could improve autism symptoms. However, the trial was withdrawn before enrolling any participants, so no new information was gathered.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- bumetanide
- What this could lead to
- If it worked, bumetanide might help reduce autism symptoms in some children.
- What could go wrong
- The trial was withdrawn before any participants enrolled, so no results are available. Earlier positive findings were small and need more confirmation.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Started
-
Dec 2016
- Finished
-
Jun 2020
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
5 to 17 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Children and teenager from age 5 to age 17, with a diagnosis of typical autism or Asperger syndrome according to the criteria of diagnosis of the WHO's classification (CIM-10), * With a known etiology, * Patients for whom the CARS results are strictly Superior or equal to 30, * Of whom the parents have given their free, informed and written consent, * Affiliated or beneficiary of the French social security. Exclusion Criteria: * Patients under treatment by inlet diuretic either at the time of the study or before, * Patients with electrolytic disorders, * Patients with a known hypersensitivity to sulfa drugs, * Patients with a hepatic or renal failure, * Patients with an epilepsy not controlled by a treatment (comitial crisis in the past 6 month at the time the trial starts despite a treatment), * Patients under treatment by psychotropic exception made of the melatonin, * Allergy to the bumetanide or one of its excipients, * Patient under a treatment by lithium, diphemanil, erythromycin IV, halofantrine, pentamidine, sultopride, vincamine, aminoglycoside, * Pregnant and lactating women. Secondary exclusion criteria: * QT prolongation noticed on the ECG at Day0, * Anomaly on the biological check up (Day 0) made before including the patient that would contraindicated the prescription of bumetanide, * Patients for whom the CARS results are strictly inferior to 30.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
CHU de Limoges
Limoges, 87042, France
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Other studies related to the condition(s) this trial covers.
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