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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01993251
Other study ID # 2012-732
Secondary ID 2013-001230-17
Status Completed
Phase Phase 2
First received
Last updated
Start date June 2014
Est. completion date June 12, 2018

Study information

Verified date January 2019
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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 timeā€¦), 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.


Recruitment information / eligibility

Status Completed
Enrollment 26
Est. completion date June 12, 2018
Est. primary completion date June 12, 2018
Accepts healthy volunteers No
Gender All
Age group 3 Years to 12 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
melatonin
one capsule, melatonin 0.5 mg, oral, once a day, 30 minutes before bedtime
Melatonin
one capsule, melatonin 2 mg, oral, once a day, 30 minutes before bedtime
Melatonin
one capsule, melatonin 6 mg, oral, once a day, 30 minutes before bedtime
placebo
one capsule, placebo, oral, once a day, 30 minutes before bedtime

Locations

Country Name City State
France Hôpital Femme Mere Enfant Bron
France CHU de Caen Caen
France Centre Hospitalier du Chinonais Chinon
France CHRU de Strasbourg Strasbourg
France CHU de Tours Tours

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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. The primary outcome will be assessed once at V2 (D29 +/- 7days) by polysomnography.
Secondary To assess in autistic children the melatonin effects on sleep characteristics by measuring the sleep latency It will be assessed once at V2 (D29 +/- 7 days) by polysomnography and actimetrics.
Secondary 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 It will be assessed once at V2 (D29 +/- 7 days) by polysomnography and actimetrics.
Secondary To assess the effectiveness of melatonin on daytime autistic behavior Evaluate the effectiveness with the rating scale autistic behavior. It will be assessed three times at V1 (D0), V2 (D29 +/- 7 days) and V4 (D44+/-7days).
Secondary To assess the melatonin safety in autistic children. Evaluate the safety with Adverse events report. It will be assessed three times at V2 (D29 +/- 7 days), V3(D30) and V4 (D44+/-7days).
Secondary Establish whether there is a correlation between sleep quality and melatonin secretion. With the urinary melatonin dosage. It will be assessed twice at V3 (D30) and V4 (D44+/-7days).
Secondary To assess in autistic children the melatonin effects on sleep characteristics. by measuring the indexes arousals at V2 (D29 +/- 7 days) by polysomnography and actimetrics.
Secondary 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 at V2 (D29 +/- 7 days) by polysomnography and actimetrics.
Secondary To assess in autistic children the melatonin effects on sleep characteristics by measuring the density of sleep spindles in light NREM sleep at V2 (D29 +/- 7 days) by polysomnography and actimetrics
Secondary To assess in autistic children the melatonin effects on sleep characteristics by measuring the density of eye movements REM sleep. at V2 (D29 +/- 7 days) by polysomnography and actimetrics.
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