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Does Melatonin Restore Sleep Architecture in Autistic Children (SOMELIA)

Primary Purpose

Sleep Disorders

Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
melatonin
Melatonin
Melatonin
placebo
Sponsored by
Hospices Civils de Lyon
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sleep Disorders focused on measuring sleep,melatonin,autism,children

Eligibility Criteria

3 Years - 12 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Boys and girls from 3 to 12 years old with autism spectrum,
  • Diagnosed by psychiatrists according to the diagnostic criteria for autism ICD-10 AND ADI or ADOS positive,
  • With trouble sleeping, assessed by questionnaire CHSQ,
  • Having made a night polysomnography,
  • Written informed consent (signed by parents),
  • Affiliated with the French universal healthcare system.

Exclusion Criteria:

  • Children who stopped all treatment for sleep for less than one month,
  • Liver or kidney insufficiencies,
  • Acute illness during or occurred in the month preceding the study,
  • Neurological disease without autism spectrum , patients with non-controlled epilepsy
  • Health background witch can influence sleep (other than autism itself),
  • Obstructive syndrome (history - oral breathing in wakefulness, nocturnal snoring significant (heard the door closed), nocturnal respiratory effort, apnea reported by parents- and clinical examination (chronic nasal congestion, large tonsils and touching),
  • Known hypersensitivity to the active substance or to one of the excipient contained in the verum or in the placebo,
  • Children under treatment against-indicated with the study treatment witch can't be stopped

Sites / Locations

  • Hôpital Femme Mere Enfant
  • CHU de Caen
  • Centre Hospitalier du Chinonais
  • CHRU de Strasbourg
  • CHU de Tours

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

melatonin 0.5mg

melatonin 2mg

melatonin 6mg

placebo

Arm Description

Outcomes

Primary Outcome Measures

To determine the most effective dose of melatonin to improve sleep quality in autistic children.
The primary outcome is to measure the awakenings index which is the number of nocturnal awakenings higher than 15 seconds per hour of sleep measured by polysomnography.

Secondary Outcome Measures

To assess in autistic children the melatonin effects on sleep characteristics
by measuring the sleep latency
To assess the effectiveness of treatment on sleep disorders.
It is to evaluate the effectiveness with the scale treatment response, the sleep questionnaire and severity index of insomnia
To assess the effectiveness of melatonin on daytime autistic behavior
Evaluate the effectiveness with the rating scale autistic behavior.
To assess the melatonin safety in autistic children.
Evaluate the safety with Adverse events report.
Establish whether there is a correlation between sleep quality and melatonin secretion.
With the urinary melatonin dosage.
To assess in autistic children the melatonin effects on sleep characteristics.
by measuring the indexes arousals
To assess in autistic children the melatonin effects on sleep characteristics.
by measuring time and percentage of different stages of NREM (Non rapid eye movement) and REM sleep
To assess in autistic children the melatonin effects on sleep characteristics
by measuring the density of sleep spindles in light NREM sleep
To assess in autistic children the melatonin effects on sleep characteristics
by measuring the density of eye movements REM sleep.

Full Information

First Posted
November 13, 2013
Last Updated
January 25, 2019
Sponsor
Hospices Civils de Lyon
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1. Study Identification

Unique Protocol Identification Number
NCT01993251
Brief Title
Does Melatonin Restore Sleep Architecture in Autistic Children
Acronym
SOMELIA
Official Title
Does Melatonin Restore Sleep Architecture in Autistic Children?
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
June 2014 (Actual)
Primary Completion Date
June 12, 2018 (Actual)
Study Completion Date
June 12, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospices Civils de Lyon

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Although behavioral disorders origins in autistic children are still unclear, they seem to be influenced by sleep disorders. Results of studies performed on sleep quality in autistic children showed a high prevalence of sleep disorders in these children, estimated between 50 and 80% compared to children with typical development and insomnia is one of the sleep disorders most frequently reported by autistic children's parents. Others studies showed circadian rhythm disorder in autistic children which could be the consequence of genetic abnormalities in the melatonin synthesis and the melatonin role in the synaptic transmission modulation. Melatonin by its sedative effects and its action on circadian pacemaker is a promoter of sleep proposed for insomnia treatment and circadian rhythm disorders. Two major recent studies (not yet published) in the United States and in England seek to show the effectiveness of melatonin by testing the effects of three doses of melatonin on reducing sleep disorders. It is therefore interesting and important to conduct a parallel study to assess the melatonin effect not only on the reduction of sleep disorders (sleep onset latency, total sleep time…), but on sleep quality (number of nocturnal awakenings). The strength of this study lies in the combination of several measurement tools to assess the melatonin dose-effect on all parameters in both physiological (actimetrics, polysomnography), biological (dosage 24h sulfatoxymelatonin), behavioral (sleep questionnaire, index of insomnia severity, rating scale autistic disorder) as well as possible side effects. The primary objective is to determine the most effective dose of melatonin to improve sleep quality in autistic children.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Disorders
Keywords
sleep,melatonin,autism,children

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
26 (Actual)

8. Arms, Groups, and Interventions

Arm Title
melatonin 0.5mg
Arm Type
Active Comparator
Arm Title
melatonin 2mg
Arm Type
Active Comparator
Arm Title
melatonin 6mg
Arm Type
Active Comparator
Arm Title
placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
melatonin
Intervention Description
one capsule, melatonin 0.5 mg, oral, once a day, 30 minutes before bedtime
Intervention Type
Drug
Intervention Name(s)
Melatonin
Intervention Description
one capsule, melatonin 2 mg, oral, once a day, 30 minutes before bedtime
Intervention Type
Drug
Intervention Name(s)
Melatonin
Intervention Description
one capsule, melatonin 6 mg, oral, once a day, 30 minutes before bedtime
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
one capsule, placebo, oral, once a day, 30 minutes before bedtime
Primary Outcome Measure Information:
Title
To determine the most effective dose of melatonin to improve sleep quality in autistic children.
Description
The primary outcome is to measure the awakenings index which is the number of nocturnal awakenings higher than 15 seconds per hour of sleep measured by polysomnography.
Time Frame
The primary outcome will be assessed once at V2 (D29 +/- 7days) by polysomnography.
Secondary Outcome Measure Information:
Title
To assess in autistic children the melatonin effects on sleep characteristics
Description
by measuring the sleep latency
Time Frame
It will be assessed once at V2 (D29 +/- 7 days) by polysomnography and actimetrics.
Title
To assess the effectiveness of treatment on sleep disorders.
Description
It is to evaluate the effectiveness with the scale treatment response, the sleep questionnaire and severity index of insomnia
Time Frame
It will be assessed once at V2 (D29 +/- 7 days) by polysomnography and actimetrics.
Title
To assess the effectiveness of melatonin on daytime autistic behavior
Description
Evaluate the effectiveness with the rating scale autistic behavior.
Time Frame
It will be assessed three times at V1 (D0), V2 (D29 +/- 7 days) and V4 (D44+/-7days).
Title
To assess the melatonin safety in autistic children.
Description
Evaluate the safety with Adverse events report.
Time Frame
It will be assessed three times at V2 (D29 +/- 7 days), V3(D30) and V4 (D44+/-7days).
Title
Establish whether there is a correlation between sleep quality and melatonin secretion.
Description
With the urinary melatonin dosage.
Time Frame
It will be assessed twice at V3 (D30) and V4 (D44+/-7days).
Title
To assess in autistic children the melatonin effects on sleep characteristics.
Description
by measuring the indexes arousals
Time Frame
at V2 (D29 +/- 7 days) by polysomnography and actimetrics.
Title
To assess in autistic children the melatonin effects on sleep characteristics.
Description
by measuring time and percentage of different stages of NREM (Non rapid eye movement) and REM sleep
Time Frame
at V2 (D29 +/- 7 days) by polysomnography and actimetrics.
Title
To assess in autistic children the melatonin effects on sleep characteristics
Description
by measuring the density of sleep spindles in light NREM sleep
Time Frame
at V2 (D29 +/- 7 days) by polysomnography and actimetrics
Title
To assess in autistic children the melatonin effects on sleep characteristics
Description
by measuring the density of eye movements REM sleep.
Time Frame
at V2 (D29 +/- 7 days) by polysomnography and actimetrics.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Boys and girls from 3 to 12 years old with autism spectrum, Diagnosed by psychiatrists according to the diagnostic criteria for autism ICD-10 AND ADI or ADOS positive, With trouble sleeping, assessed by questionnaire CHSQ, Having made a night polysomnography, Written informed consent (signed by parents), Affiliated with the French universal healthcare system. Exclusion Criteria: Children who stopped all treatment for sleep for less than one month, Liver or kidney insufficiencies, Acute illness during or occurred in the month preceding the study, Neurological disease without autism spectrum , patients with non-controlled epilepsy Health background witch can influence sleep (other than autism itself), Obstructive syndrome (history - oral breathing in wakefulness, nocturnal snoring significant (heard the door closed), nocturnal respiratory effort, apnea reported by parents- and clinical examination (chronic nasal congestion, large tonsils and touching), Known hypersensitivity to the active substance or to one of the excipient contained in the verum or in the placebo, Children under treatment against-indicated with the study treatment witch can't be stopped
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Patricia Franco, MD
Organizational Affiliation
CHU Hôpital Femme Mère Enfant.Bron
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Femme Mere Enfant
City
Bron
ZIP/Postal Code
69677
Country
France
Facility Name
CHU de Caen
City
Caen
ZIP/Postal Code
14033
Country
France
Facility Name
Centre Hospitalier du Chinonais
City
Chinon
Country
France
Facility Name
CHRU de Strasbourg
City
Strasbourg
ZIP/Postal Code
67091
Country
France
Facility Name
CHU de Tours
City
Tours
ZIP/Postal Code
37044
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No

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Does Melatonin Restore Sleep Architecture in Autistic Children

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