Melatonin Dose-effect Relation in Childhood Autism (MELADOSE)
Primary Purpose
Childhood Autism
Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
melatonin
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Childhood Autism focused on measuring melatonin, childhood autism, 6-Sulphatoxymelatonin, autistic disorder, dose-effect relation
Eligibility Criteria
Inclusion Criteria:
- Prepubertal males with autism from 6 to 8 years old, according to the diagnostic criteria of autistic disorder of the WHO (CIM-10), American (DSM-IV-TR) and French (CFTMEA) classifications.
- Verbal language level required for the ADOS (Module 1) (i.e., no verbal language as defined by the ADI-R (autism diagnostic interview-revised) scale).
- Written informed consent of the parents or the legal representative.
Non-inclusion Criteria:
- Treatment by benzodiazepines.
- Treatment by anticonvulsant drugs.
- Treatment by serotoninergic products.
- Hypersensitivity reaction to the active substance or one of the excipients of the product.
- Patient with hereditary galactose intolerance, Lapp lactase deficiency or malabsorption syndrome of glucose and galactose.
- Children who are not able to swallow tablets.
Sites / Locations
- Service de Psychiatrie de l'Enfant et de l'Adolescent - Hôpital de la Pitié-Salpêtrière
- Centre Hospitalier Spécialisé Henri Laborit
- Service de Psychothérapie de l'Enfant et de l'Adolescent - Hôpital Robert Debré
- Pôle de Psychiatrie de l'Enfant et de l'Adolescent - Centre Hospitalier Guillaume Régnier
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Placebo Comparator
Experimental
Experimental
Experimental
Arm Label
Placebo
2 mg melatonin
4 mg melatonin
10 mg melatonin
Arm Description
5 tablets of placebo once a day, an hour before falling asleep, for 6 weeks.
1 tablet of 2mg melatonin and 4 tablets of its placebo once a day, an hour before falling asleep, for 6 weeks.
2 tablets of 2mg melatonin and 3 tablets of its placebo once a day, an hour before falling asleep, for 6 weeks.
5 tablets of 2mg melatonin once a day, an hour before falling asleep, for 6 weeks.
Outcomes
Primary Outcome Measures
Severity of autistic disorder
Secondary Outcome Measures
Severity of autistic impairments
Severity of autistic impairments (global severity of autistic disorder and anxiety) using the ADOS (Autism Diagnostic Observation Scale)
Sleep problems
Sleep problems will be assessed using a parental questionnaire and an actimetry sensor in the child recording
Excretion of the urinary metabolite of melatonin
Diurnal and nocturnal excretion of the urinary metabolite of melatonin (6-Sulphatoxymelatonin)
Severity of autistic impairments
Severity of autistic impairments (global severity of autistic disorder and anxiety) using the ICG scale
Severity of autistic impairments
Severity of autistic impairments (global severity of autistic disorder and anxiety) using the ADOS (Autism Diagnostic Observation Scale)
Sleep problems
Sleep problems will be assessed using a parental questionnaire and an actimetry sensor in the child recording
Excretion of the urinary metabolite of melatonin
Diurnal and nocturnal excretion of the urinary metabolite of melatonin (6-Sulphatoxymelatonin)
Severity of autistic impairments
Severity of autistic impairments (global severity of autistic disorder and anxiety) using the ICG scale
Full Information
NCT ID
NCT01780883
First Posted
January 25, 2013
Last Updated
May 22, 2023
Sponsor
Rennes University Hospital
Collaborators
Centre Hospitalier Guillaume Régnier, RENNES
1. Study Identification
Unique Protocol Identification Number
NCT01780883
Brief Title
Melatonin Dose-effect Relation in Childhood Autism
Acronym
MELADOSE
Official Title
Melatonin Dose-effect Relation in Childhood Autism
Study Type
Interventional
2. Study Status
Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
February 2013 (undefined)
Primary Completion Date
July 2013 (Actual)
Study Completion Date
September 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Rennes University Hospital
Collaborators
Centre Hospitalier Guillaume Régnier, RENNES
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Melatonin is a neurohormone produced from serotonin which promotes sleep. The alterations in central and peripheral serotonin neurobiology and in circadian sleep-wake rhythms observed in autistic disorder suggest abnormalities in melatonin secretion.
Several studies have reported a decrease in melatonin secretion in individuals with autism. Furthermore, nocturnal excretion of 6-Sulphatoxymelatonin (the predominant melatonin metabolite) was significantly negatively correlated with severity of autistic impairments in verbal communication and play. Melatonin could therefore have a therapeutic effect on sleep problems and may play a role in the pathophysiology of autistic disorder.
These data highlight the possible therapeutic interest of an oral administration of melatonin in patients with autistic disorder. Thus, the objective of this clinical trial is to study the relation between the melatonin dose administered and its effect on severity of autistic impairments especially in verbal communication and play.
Detailed Description
The hormone melatonin is of interest in autism due to theoretical considerations and reports of altered melatonin production in individuals with autism. Melatonin produced in the pineal gland helps regulate human circadian rhythms including sleep-wake, and is considered as the best measure of circadian rhythms.
Several studies revealed that plasmatic and urinary nocturnal levels of melatonin are significantly lower in individuals with autism (in particular, in prepubertal children) compared to typically developing individuals. In addition, this reduction in nocturnal melatonin was significantly associated with the severity of communication and social interaction impairments, especially in verbal communication and play. Finally, diurnal excretion of melatonin was also found to be decreased in individuals with autistic disorder.
Given these results, administration of melatonin could serve, at least in prepubertal children wih autism, to normalize physiological, developmental and behavioral processes that are influenced by this pineal hormone. A randomized clinical trial is therefore necessary to establish potential therapeutic efficacy of melatonin in autistic disorder and to specify its dose-effect relation. This is the first clinical trial studying the melatonin dose-effect in autism.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Childhood Autism
Keywords
melatonin, childhood autism, 6-Sulphatoxymelatonin, autistic disorder, dose-effect relation
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
34 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
5 tablets of placebo once a day, an hour before falling asleep, for 6 weeks.
Arm Title
2 mg melatonin
Arm Type
Experimental
Arm Description
1 tablet of 2mg melatonin and 4 tablets of its placebo once a day, an hour before falling asleep, for 6 weeks.
Arm Title
4 mg melatonin
Arm Type
Experimental
Arm Description
2 tablets of 2mg melatonin and 3 tablets of its placebo once a day, an hour before falling asleep, for 6 weeks.
Arm Title
10 mg melatonin
Arm Type
Experimental
Arm Description
5 tablets of 2mg melatonin once a day, an hour before falling asleep, for 6 weeks.
Intervention Type
Drug
Intervention Name(s)
melatonin
Other Intervention Name(s)
Circadin®
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo tablets of Circadin®
Primary Outcome Measure Information:
Title
Severity of autistic disorder
Time Frame
6 weeks after the beginning of the treatment.
Secondary Outcome Measure Information:
Title
Severity of autistic impairments
Description
Severity of autistic impairments (global severity of autistic disorder and anxiety) using the ADOS (Autism Diagnostic Observation Scale)
Time Frame
3 weeks after the beginning of the treatment
Title
Sleep problems
Description
Sleep problems will be assessed using a parental questionnaire and an actimetry sensor in the child recording
Time Frame
3 weeks after the beginning of the treatment
Title
Excretion of the urinary metabolite of melatonin
Description
Diurnal and nocturnal excretion of the urinary metabolite of melatonin (6-Sulphatoxymelatonin)
Time Frame
3 weeks after the beginning of the treatment
Title
Severity of autistic impairments
Description
Severity of autistic impairments (global severity of autistic disorder and anxiety) using the ICG scale
Time Frame
3 weeks after the beginning of the treatment
Title
Severity of autistic impairments
Description
Severity of autistic impairments (global severity of autistic disorder and anxiety) using the ADOS (Autism Diagnostic Observation Scale)
Time Frame
6 weeks after the beginning of the treatment
Title
Sleep problems
Description
Sleep problems will be assessed using a parental questionnaire and an actimetry sensor in the child recording
Time Frame
6 weeks after the beginning of the treatment
Title
Excretion of the urinary metabolite of melatonin
Description
Diurnal and nocturnal excretion of the urinary metabolite of melatonin (6-Sulphatoxymelatonin)
Time Frame
6 weeks after the beginning of the treatment
Title
Severity of autistic impairments
Description
Severity of autistic impairments (global severity of autistic disorder and anxiety) using the ICG scale
Time Frame
6 weeks after the beginning of the treatment
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
8 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Prepubertal males with autism from 6 to 8 years old, according to the diagnostic criteria of autistic disorder of the WHO (CIM-10), American (DSM-IV-TR) and French (CFTMEA) classifications.
Verbal language level required for the ADOS (Module 1) (i.e., no verbal language as defined by the ADI-R (autism diagnostic interview-revised) scale).
Written informed consent of the parents or the legal representative.
Non-inclusion Criteria:
Treatment by benzodiazepines.
Treatment by anticonvulsant drugs.
Treatment by serotoninergic products.
Hypersensitivity reaction to the active substance or one of the excipients of the product.
Patient with hereditary galactose intolerance, Lapp lactase deficiency or malabsorption syndrome of glucose and galactose.
Children who are not able to swallow tablets.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sylvie TORDJMAN, MD, PhD
Organizational Affiliation
Centre Hospitalier Guillaume Régnier, RENNES
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Eric BELLISSANT, MD, PhD
Organizational Affiliation
Rennes University Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Service de Psychiatrie de l'Enfant et de l'Adolescent - Hôpital de la Pitié-Salpêtrière
City
Paris
ZIP/Postal Code
75013
Country
France
Facility Name
Centre Hospitalier Spécialisé Henri Laborit
City
Poitiers
ZIP/Postal Code
86280
Country
France
Facility Name
Service de Psychothérapie de l'Enfant et de l'Adolescent - Hôpital Robert Debré
City
Reims
ZIP/Postal Code
51092
Country
France
Facility Name
Pôle de Psychiatrie de l'Enfant et de l'Adolescent - Centre Hospitalier Guillaume Régnier
City
Rennes
ZIP/Postal Code
35200
Country
France
12. IPD Sharing Statement
Citations:
PubMed Identifier
28503116
Citation
Tordjman S, Chokron S, Delorme R, Charrier A, Bellissant E, Jaafari N, Fougerou C. Melatonin: Pharmacology, Functions and Therapeutic Benefits. Curr Neuropharmacol. 2017 Apr;15(3):434-443. doi: 10.2174/1570159X14666161228122115.
Results Reference
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Melatonin Dose-effect Relation in Childhood Autism
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