Melatonin for chronic sleep onset insomnia in children: A randomized placebo-controlled trial

Citation
Mg. Smits et al., Melatonin for chronic sleep onset insomnia in children: A randomized placebo-controlled trial, J CHILD NEU, 16(2), 2001, pp. 86-92
Citations number
39
Categorie Soggetti
Pediatrics,"Neurosciences & Behavoir
Journal title
JOURNAL OF CHILD NEUROLOGY
ISSN journal
08830738 → ACNP
Volume
16
Issue
2
Year of publication
2001
Pages
86 - 92
Database
ISI
SICI code
0883-0738(200102)16:2<86:MFCSOI>2.0.ZU;2-8
Abstract
To establish the efficacy of melatonin treatment in childhood sleep onset i nsomnia, 40 elementary school children, 6 to 12 years of age, who suffered more than 1 year from chronic sleep onset insomnia, were studied in a doubl e-blind, placebo-controlled study. The children were randomly assigned to r eceive either 5-mg melatonin or placebo. The study consisted of a 1-week ba seline, consecutively followed by a 4-week treatment period. After that per iod, treatment was continued if the parents wished so. The study's impact w as assessed by measurements of lights-off time, sleep onset, and wake-up ti me, recorded in a diary (n = 33). Sleep onset was also recorded with an act igraph (n = 25). Endogenous dim light melatonin onset was measured in saliv a (n = 27). Sustained attention was evaluated with the Bourdon-Vos reaction time test (n = 36). In the melatonin group, mean (95% Cl) lights-off time advanced 34 (6-63) minutes, diary sleep onset 63 (32-94) minutes, actigraph ic sleep onset 75 (36-114) minutes, and melatonin onset 57 (24 to 89) minut es; total sleep time increased 41 (19-62) minutes. In the placebo group, th ese parameters did not shift significantly. The change during the 4-week tr eatment period differed between the treatment groups significantly as to li ghts-off time, diary and actigraphic sleep onset, sleep duration, and melat onin onset. There were no significant differences between the treatment gro ups in the change of sleep latency, wake-up time, and sustained attention r eaction times. Mild headache occurred in 2 children during the first 2 days of the melatonin treatment. Eighteen months after the start of the trial, in 13 of the 38 children who could be followed up, melatonin treatment was stopped because their sleep problem was solved and in I child because sleep was not improved. Twelve children used melatonin 5 mg, the other 1.0 to 2. 5 mg. One child developed mild generalized epilepsy 4 months after the star t of the trial. The results show that melatonin, 5 mg at 6 Pm, was relative ly safe to take in the short term and significantly more effective than pla cebo in advancing sleep onset and dim light melatonin onset and increasing sleep duration in elementary school children with chronic sleep onset insom nia. Sustained attention was not affected.