Long Term Treatment With Zolpidem: Nightly and Intermittent Dosing
Insomnia, Primary Insomnia, Psychophysiologic Insomnia
About this trial
This is an interventional treatment trial for Insomnia focused on measuring Insomnia, Sleep, zolpidem, Ambien, Hypnotics
Eligibility Criteria
Inclusion Criteria: Ages 25 - 55 a stable sleep/wake schedule with a preferred sleep phase between 10:00 p.m. and 8:00 a.m. Patients with Primary Insomnia will meet diagnostic criteria for Psychophysiologic Insomnia according to the International Classification of Sleep Disorders manual (ICSD). complaint of disturbed sleep must have the following characteristics: >30 minutes to fall asleep, and/or >30 minutes wake after sleep onset time, a total sleep time of no more than 6.5 hours (or a sleep efficiency of less than 85%), a problem frequency of >4 nights/ week and a problem duration >6 months. Exclusion Criteria: Unstable medical or psychiatric illness Use of medication that may cause insomnia or may be reduce the effectiveness of zolpidem (e.g. selective serotonin reuptake inhibitors(SSRI's), steroids, bronchodilators, calcium channel blockers, beta blockers, etc.) symptoms suggestive of sleep disorders other than insomnia polysomnographic data indicating sleep disorders other than insomnia Evidence of active illicit substance use or fitting criteria for alcohol abuse or dependence inadequate language comprehension pregnancy first-degree relatives with bipolar disorder or schizophrenia
Sites / Locations
- University of Rochester Sleep Research Laboratory
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Placebo Comparator
Active Comparator
Experimental
No Intervention
Placebo
QHS Zolpidem
Intermittant Zolpidem
Control
QHS dosing with placebo (i.e. nightly dose)
QHS dosing with 10mg of zolpidem (i.e. nightly dose)
Intermittent dosing with 10mg of zolpidem (3-5 pills per week as needed
Monitor only condition (no placebo, no drug).