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Trial record 5 of 14 for:    bumetanide

Efficacy and Safety of Bumetanide Oral Liquid Formulation in Children Aged From 2 to Less Than 7 Years Old With Autism Spectrum Disorder.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT03715153
Recruitment Status : Recruiting
First Posted : October 23, 2018
Last Update Posted : July 8, 2020
ADIR, a Servier Group company
Information provided by (Responsible Party):
Servier ( Institut de Recherches Internationales Servier )

Brief Summary:
The purpose of this study is to evaluate the efficacity and the safety of bumetanide/S95008 in the improvement of Autism Spectrum Disorder core symptoms.

Condition or disease Intervention/treatment Phase
Autism Spectrum Disorder (ASD) Drug: BUMETANIDE/S95008 Drug: PLACEBO Phase 3

Detailed Description:
The present study (CL3-95008-002) will be performed in children from 2 to less than 7 years old presenting with ASD. A 6-month double-blind treatment period will be performed in which efficacy and safety of bumetanide 0.5mg BID will be assessed versus placebo. This double-blind period will be followed by a 6-month open label treatment period of bumetanide 0.5mg BID in which long term safety will be evaluated.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 200 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: 6-month, randomized, double-blind, placebo-controlled, parallel groups followed by an open label active 6-month treatment period with bumetanide.
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Efficacy and Safety of Bumetanide Oral Liquid Formulation in Children Aged From 2 to Less Than 7 Years Old With Autism Spectrum Disorder. A 6-month Randomised, Double-blind, Placebo Controlled Multicentre Parallel Group Study to Evaluate Efficacy and Safety of Bumetanide 0.5mg Twice a Day Followed by an Open Label Active 6-month Treatment Period With Bumetanide (0.5mg Twice a Day) and a 6 Weeks Discontinuation Period After Treatment Stop.
Actual Study Start Date : October 4, 2018
Estimated Primary Completion Date : August 2021
Estimated Study Completion Date : April 2022

Resource links provided by the National Library of Medicine

Drug Information available for: Bumetanide

Arm Intervention/treatment
Experimental: BUMETANIDE/S95008 Drug: BUMETANIDE/S95008
Oral solution dosed at 0.5 mg/mL Taken twice daily.

Placebo Comparator: PLACEBO Drug: PLACEBO
Oral solution Taken twice daily.

Primary Outcome Measures :
  1. Childhood Autism Rating Scale, Second Edition (CARS2) total raw score [ Time Frame: change from baseline to 6 month ]
    Efficacy criterion The CARS2 is a 15 item rated instrument. The rating values given for the 15 areas are summed to produce a Total score.

Secondary Outcome Measures :
  1. Social Responsiveness Scale, Second Edition (SRS-2) total raw score [ Time Frame: Change from baseline to 6 month ]
    Efficacy criterion 65 items scale measuring symptoms associated with autism

  2. Clinical Global Impression - Global Improvement (CGI-I) score [ Time Frame: At 6 months ]
    Efficacy criterion Scale which assesses the severity of the illness and the global improvement of the patient Under study treatment

  3. Vineland Adaptative Behaviour Scale II (VABS II) [ Time Frame: Change from baseline to 6 month ]
    Efficacy criterion Scale designated to measure adaptative behaviour

  4. Adverse Event and Pediatric Adverse Event Rating Scale (PAERS) [ Time Frame: On average of 52 weeks ]
    Safety criterion Inventory report used to identify signs/symptoms experienced by the patient since the study treatment initiation.

  5. Abnormalities in 12-leads electrocardiogram (ECG) parameters [ Time Frame: Selection visit, Week004, Week008, Week012, Week026, Week030, Week034, Week038, Week052 ]
    Safety criterion

  6. Renal ultrasound [ Time Frame: Selection visit, Week026, Week052 ]
    Safety criterion Assessment of the renal function

  7. Columbia-Suicide severity scale Children's version (C-SSRS-C) [ Time Frame: Week000/Week012/Week026/Week038/Week052 ]
    Scale which assesses suicidal ideation and suicidal behaviour

  8. Acceptability and palatability questionnaires [ Time Frame: Week026 ]
    Acceptability and palatability criterion Assessment of the ease of use to use the dosing device

  9. Paediatric Quality of Life Inventory (PedsQL) questionnaire [ Time Frame: Week000/Week004/Week012/v026/Week030/Week038/Week052 ]
    Quality of Life questionnaire Assessment of parent/legal representative perception of patient health related quality of life

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Ages Eligible for Study:   2 Years to 6 Years   (Child)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Male and female patients from 2 to less than 7
  • Primary diagnosis of ASD as per Diagnostic and Statistical Manual of Mental Disorders - Fifth Edition (DSM-5) criteria
  • Criteria met for ASD on Autism Diagnostic Observation Schedule-Generic (ADOS-2) and Autism Diagnosis Interview Revised (ADI-R)
  • CGI (Clinical Global Impression) - Severity rating Score ≥ 4
  • Childhood Autism Rating Scale second edition (CARS2-ST or HF) total raw score ≥ 34
  • Social responsiveness Scale second edition (SRS-2) total score ≥ 66 T-Score
  • Absence of diagnosis of Fragile X or Rett Syndrome
  • Absence of any clinically significant abnormality likely to interfere with the conduct of the study according to the judgment of the investigator.

Exclusion Criteria:

  • Patients not able to follow the study assessments defined by the protocol, with the exception of self-rating questionnaires which will be assessed by parent/legal representative/caregiver for those patients unable to complete them
  • Patients having a high suicidal risk according to the investigator judgement
  • Chronic renal dysfunction
  • Chronic cardiac dysfunction
  • Patient with unstable psychotherapy, behavioural, cognitive or cognitive-behavioural therapy
  • Severe electrolyte imbalance that is likely to interfere with the study conduct or evaluation

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT03715153

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Contact: Institut de Recherches Internationales Servier Clinical Studies Department +33 1 55 72 43 66

Hide Hide 55 study locations
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United States, Nevada
Center for Psychiatry and Behavioral Medicine Not yet recruiting
Las Vegas, Nevada, United States, 89128
United States, New York
Richmond Behavioral Associates Not yet recruiting
Staten Island, New York, United States, 10312
Liverpool Hospital Recruiting
Liverpool, Australia, 2170
Contact    +61 491 619 216   
The Royal Children's Hospital Melbourne Recruiting
Parkville, Australia, 3052
Trial Tech em Pesquisas com Medicamentos Ltda Recruiting
Curitiba, Brazil, 80240-280
Hospital Universitário Walter Cantídio-Universidade Federal do Ceará Recruiting
Fortaleza, Brazil, 60430-370
Clínica Neurológica e Neurocirúrgica de Joinville Recruiting
Joinville, Brazil, 89202-190
Contact    +55 47 3451-2596   
Hospital São Vicente de Paulo Recruiting
Passo Fundo, Brazil, 99010-080
Universidade Federal de São Paulo, Escola Paulista de Medicina Recruiting
São Paulo, Brazil, 04017-030
Faculdade de Medicina da Universidade de São Paulo - Departamento de psiquiatra Recruiting
São Paulo, Brazil, 054030-010
Contact: Helena Brentani    55 11 2661-6978   
University hospital of Ostrava, Department of Psychiatry Recruiting
Poruba, Ostrava, Czechia
Contact    +4 2 0597373280   
University Hospital Brno, Department of Child Neurology Recruiting
Brno, Czechia, 613 00
Institute of Neuropsychiatric Care, Department of Child Psychiatry Recruiting
Praha, Czechia, 186 00
Contact    +4 2 0739226131   
GSC CHU-LENVAL Centre ressource autisme Recruiting
Nice, Alpes-Maritimes, France, 6200
Contact: Sylvie Serret    +33 04 92 03 04 39    serret.s@pé   
Hôpitaux Universitaires de Strasbourg Service de Psychiatrie de l'Enfant et de l'Adolescent Recruiting
Strasbourg, Alsace-Champagne-Ardenne-Lorraine, France, 67091
Contact: Isabelle Ohresser    +33 3 88 11 52 48   
Centre d'Investigation Clinique de Lyon Recruiting
Bron, Auvergne Rhone Alpes, France, 69677
Contact: sandrine mardirossian   
Hôpital Le Vinatier CRA Rhône-Alpes, Bat 211 Recruiting
Bron Cedex, Auvergne-Rhône-Alpes, France, 69678
Contact: Sandrine Mardirossian   
Hôpital Robert Debré Service de Psychiatrie de l'enfant et de l'adolescent Recruiting
Paris, Ile De France, France, 75019
Contact: Richard DELORME    +33 1 40 03 23 00   
CHU Rouen Recruiting
Rouen, Normandie, France, 76000
Contact: Nathalie Mestre    02 32 88 57 84   
Centre Hospitalier du Rouvray Centre de Ressources pour l'Autisme Recruiting
Sotteville-lès-Rouen, Normandie, France, 76301
Contact: Nathalie Mestre    +33 2 32 88 57 84   
Hôpital des Enfants-Pellegrin Recruiting
Bordeaux, Nouvelle Aquitaine, France, 33076
Contact: Manuel Bouvard    +33   
Centre Hospitalier Charles Perrens CRA Aquitaine Recruiting
Bordeaux, Nouvelle-Aquitaine, France, 33076
Contact: Manuel BOUVARD    +33 5 56 56 17 19   
Universitätsklinikum Freiburg, Zentrum für Psychische Erkrankungen, Klinik für Psychiatrie, Psychotherapie und Psychosomatik im Kindes- und Jugendalter Withdrawn
Freiburg, Baden-Württemberg, Germany, 79104
Klinik für Psychiatrie und Psychotherapie des Kindes- und Jugendalters am Zentralinstitut für Seelische Gesundheit Withdrawn
Mannheim, Baden-Württemberg, Germany, 68159
Universitätsklinikum Tübingen, Abt. Psychiatrie, Psychosomatik und Psychotherapie im Kindes- und Jugendalter Withdrawn
Tuebingen, Baden-Württemberg, Germany, 72076
Universitätsklinikum Carl Gustav Carus an der TU Dresden, Klinik und Poliklinik für Kinder- und Jugendpsychiatrie und-psychotherapie Withdrawn
Dresden, Saxony (Sachsen), Germany, 01307
Vadaskert Korhaz es Szakambulancia Recruiting
Budapest, Hungary, 1021
Contact: Péter Nagy    +36 1 392 1400      
Servus Salvus Fft. Recruiting
Budapest, Hungary, 1026
Contact: Anna Altmann   
Magyar Református Egyház Bethesda Gyermekkórháza Recruiting
Budapest, Hungary, 1143
Bekes Megyei Kozponti Korhaz Gyermek es ifjusagpszichiatriai osztaly Recruiting
Gyula, Hungary, 5700
Contact: Magdolna Gácser         
Szegedi Tudományegyetem Szent-Gyorgy Albert Klinikai Kozpont Gyermekgyógyászati Klinika Gyermek es Ifjusagpszichiátriai o Recruiting
Szeged, Hungary, 6725
Contact: Krisztina Kapornai         
Neuro Riabilitazione/Psicopatologia dell'età evolutiva Istituto Scientifico Medea - Bosisio Parini Recruiting
Bosisio Parini, Lombardia, Italy, 23842
Contact    +39 031 877584   
U.O. di Neuropsichiatria Infantile Fondazione Istituto Neurologico Nazionale Casimiro Mondino Istituto di Ricovero e Cura a Carattere Scientifico Recruiting
Pavia, Lombardia, Italy, 27100
Contact: Martina Maria Mensi    +39 0382 380242   
Clinica di Neuropsichiatria dell'Infanzia e dell'Adolescenza Ospedale Pediatrico-Microcitemico Recruiting
Cagliari, Sardegna, Italy, 09131
Contact: Caterina Medda    +39 070 52963512   
Programma Interdipartimentale "Autismo 0-90" A.O.U. Policlinico "Gaetano Martino" Recruiting
Messina, Sicilia, Italy, 98125
U.O.C. Psichiatria dello Sviluppo IRCCS Fondazione Stella Maris Recruiting
Calambrone, Toscana, Italy, 56128
Contact: Elisa Santocchi    +39 050 88 63 13   
U.O. di Neuropsichiatria Infantile Azienda Ospedaliera Universitaria Senese Recruiting
Siena, Toscana, Italy, 53100
Contact: Roberto Canitano   
"Niepubliczny Zakład Opieki Zdrowotnej Gdańskie Centrum Zdrowia Sp. z o.o. Recruiting
Gdansk, Poland, 80-542
Contact    + 48 58 342-34-08      
Centrum Badań Klinicznych PI-House sp. z o.o Recruiting
Gdansk, Poland, 80-546
Contact    +48 58 719 22 22   
NAVICULA Centrum Diagnozy i Terapii Autyzmu w Łodzi Recruiting
Lodz, Poland, 91-126
Contact    +(48)42-611-83-45   
Fundacja SYNAPSIS ul. Recruiting
Warszawa, Poland, 02-085
Contact    +48 22 825-87-42   
Samodzielny Publiczny Dziecięcy Szpital Kliniczny w Warszawie Oddział Kliniczny Psychiatrii Wieku Rozwojowego Recruiting
Warszawa, Poland, 02-091
Contact    +(48) 22 317 92 51   
Centro Hospitalar e Universitario de Coimbra Hospital Pediatrico Recruiting
Coimbra, Portugal, 300-062
Contact: Guiomar Oliveira    + 351 96 554 7899   
National Institute of Children Diseases, Department of Child Psychiatry Recruiting
Bratislava, Slovakia, 833 40
Contact    +42 1 259371508   
EPAMED, s.r.o. Recruiting
Košice, Slovakia, 040 01
Hospita Mutua de Terrassa Recruiting
Terrassa, Barcelona, Spain, 08221
Contact: Amaia Hervas   
Policlinica Guipuzcoa Recruiting
San Sebastian, Guipuzcoa, Spain, 20014
Hospital Puerta de Hierro Recruiting
Majadahonda, Madrid, Spain, 28222
Contact: Inmaculada Palanca   
Usm Infantil Benalua Recruiting
Alicante, Spain, 03007
Contact: Auxiliadora Javaloyes   
Hospital Clinic de Barcelona Recruiting
Barcelona, Spain, 08036
Contact: Rosa María Calvo Escalona    00 34 93 227 54 00 ext 4212   
Hospital Niño Jesus Recruiting
Madrid, Spain, 28009
Contact: Silvia Gutierrez Priego    00 34 91 5035900 ext 351   
Hospital Universitario Gregorio Marañon Recruiting
Madrid, Spain, 28009
United Kingdom
Colchester Hospital Recruiting
Colchester, United Kingdom, CO4 5JL
Contact    +44 (0)120 6746 285   
ReCognition Health Recruiting
London, United Kingdom, W1G 9JF
The Winnicott Centre 195-197 Hathersage Road Recruiting
Manchester, United Kingdom, M13 0JE
Sponsors and Collaborators
Institut de Recherches Internationales Servier
ADIR, a Servier Group company
Additional Information:
Study Data/Documents: Individual Participant Data Set  This link exits the site

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Responsible Party: Institut de Recherches Internationales Servier Identifier: NCT03715153    
Other Study ID Numbers: CL3-95008-002
2017-004420-30 ( EudraCT Number )
First Posted: October 23, 2018    Key Record Dates
Last Update Posted: July 8, 2020
Last Verified: July 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description:

Qualified scientific and medical researchers can request access to anonymized patient-level and study-level clinical trial data.

They can ask for all interventional clinical studies:

  • submitted for new medicines and new indications approved after 1 January 2014 in the European Economic Area (EEA) or the United States (US).
  • Where Servier or an affiliate are the Marketing Authorization Holders (MAH). The date of the first Marketing Authorization of the new médicine (or the new indication) in one of the EEA Member States will be considered within this scope.
Supporting Materials: Study Protocol
Statistical Analysis Plan (SAP)
Informed Consent Form (ICF)
Clinical Study Report (CSR)
Time Frame: After Marketing Authorisation in EEA or US if the study is used for the approval.
Access Criteria: Researchers should register on Servier Data Portal and fill in the research proposal form. This form in four parts should be fully documented. The Research Proposal Form will not be reviewed until all mandatory fields are completed.

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Autistic Disorder
Autism Spectrum Disorder
Child Development Disorders, Pervasive
Neurodevelopmental Disorders
Mental Disorders
Natriuretic Agents
Physiological Effects of Drugs
Sodium Potassium Chloride Symporter Inhibitors
Membrane Transport Modulators
Molecular Mechanisms of Pharmacological Action