This study examined rebound insomnia after discontinuation of chronic
use of zolpidem (10 mg), a short elimination half-life imidazopyridine
. The zolpidem group was bracketed by a placebo,stoup and a positive c
ontrol group taking 0.5 mg of triazolam (twice the recommended dose),
which is known to produce rebound insomnia. Ninety-nine patients with
sleep complaints that were polysomnographically documented participate
d in the study. After randomization, patients completed a 2-night, sin
gle-blind, placebo baseline period, a 28-night double-blind treatment
phase, and a 3-night, single-blind, placebo substitution period. Polys
omnographic and subjective sleep variables indicated a lack of rebound
insomnia for the zolpidem group. The positive triazolam control group
had rebound insomnia only on the first discontinuation night. There w
as no significant correlation between rebound insomnia and the level o
f initial insomnia, the degree of response to treatment in week 4, or
the amount of tolerance that developed during drug use. During the 4-w
eek treatment period, efficacy diminished for both drugs. From these d
ata, it cannot be determined whether the lack of rebound insomnia with
zolpidem is a result of drug dose or some property of the drug such a
s receptor selectivity.