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CompletedNCT03492970SMS-adultsUpdated Apr 22, 2019

Melatonin in Adults With SMS

An interventional study of Hourly dosing of the nychtemeral secretion of melatonin in Smith Magenis Syndrome, sponsored by Hôpital le Vinatier. Completed at 1 site in France. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2019-04-22.

Sponsored by Hôpital le Vinatier · Not applicable, Interventional, and Screening

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Phase
Not applicable
Study type
Interventional
Enrollment
10
Allocation
Not applicable
Ages
18 Years to 65 Years
Sex
All
01

Study summary

Sleep-Wake and behavioral disorders in Smith Magenis Syndrome (SMS) are strongly linked to an inversion of the nychtemeral secretion of melatonin. This inversion have been described in children with SMS. However its evolution during adulthood remains unknown. The aim of this study is to assess 24hours melatonin levels in 10 adults with SMS in order to optimize medication in adults with SMS

Read the detailed description

SMS is one of the rare syndromes in which the inversion of melatonin secretion is regular, which is an exceptional situation for the study of the influence of genetic factors on the regulation of sleep / wake rhythm. Recently, point mutations of the RAI1 gene (Retinoic Acid Induced 1) have been identified in individuals with the clinical features of SMS with a reversal of the secretion rate of melatonin ,highlighting the role of RAI1 in SMS sleep disorders.

Daytime secretion of melatonin is associated with significant drowsiness and plays a major role in diurnal behavior disorders, especially in younger people. Conversely, the absence of nocturnal melatonin is a causal factor in the shortening and fragmentation of nocturnal sleep .

Basically, little is known about the mechanisms that explain the inversion of the secretion rate of melatonin in SMS.

These aspects, and in particular the nycthemeral reversal of the melatonin cycle, have been described in a population of children and we do not know how these disturbances evolve in adulthood

02

Conditions studied

  • Smith Magenis Syndrome
03

In context

Lead sponsor

Hôpital le Vinatier is the lead sponsor of 106 studies on the registry; 41 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patient with Smith Magenis Syndrome aged 18 years or older
  • subject or guardian having signed the consent

Exclusion criteria

Exclusion Criteria:

  • Pregnant women
  • Minor subject
  • Diagnosis of Smith Magenis syndrome not certain
  • Taking benzodiazepines or related substances
  • Taking betablockers
  • Major behavioral disorders versus indicating participation in this study
05

Study design

Phase
Not applicable
Primary purpose
Screening
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
10 participants (actual)

Study arms

  • Other
    10 adult patients with SMS

    Specify the evolution of the nycthemeral cycle of melatonin secretion in adult subjects carrying an SMS Behavioral characterization of adult subjects with SMS Make recommendations on the management of sleep / sleep rhythm disorders and behavior in adult subjects with SMS

    Biological: Hourly dosing of the nychtemeral secretion of melatonin

Interventions

  • BiologicalHourly dosing of the nychtemeral secretion of melatonin

    Hourly dosing of the nychtemeral secretion of melatonin links and with sleep disorders and behavior of adult patients with SMS

06

What researchers measure

Primary outcomes

  1. 24h melatonin levels

    Plasmatic melatonin level will be assessed every hour during 24h for each subject

    Time frame: 24 hours

Secondary outcomes

  1. Analysis of actimetry

    At the end of the Visit 1 interview, an actimeter will be given to the patient to be worn on the previous two weeks before Visit 2. This will allow the evaluation of the sleep / wake rhythm in the usual life situation. The actimeter will be reported by the patient during the second visit .

    Time frame: 15 days

07

Study locations

1 site
  • CH Le Vinatier
    BRON Cedex, Rhône-Alpes 69678, France
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Mar 2018 to primary completion in Jan 2019, 10 months.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 1, 2018
First posted
Apr 10, 2018
StartActual
Mar 7, 2018
Primary completionActual
Jan 30, 2019
CompletionActual
Mar 30, 2019
Last update
Apr 22, 2019
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 22, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03492970
Responsible party
Sponsor
First posted
Apr 10, 2018
Start date
Mar 7, 2018
Primary completion
Jan 30, 2019
Completion
Mar 30, 2019
Last update
Apr 22, 2019

Study contacts

POISSON ALICE, PH
principal investigator · CH LE VINATIER

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Apr 2019. You cannot join it, but the record below documents what was studied.

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