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Chesterfield, Missouri 63017


Purpose:

The purpose of this study is to determine the effect of two hypnotic medications, zolpidem extended release and zaleplon, on memory. It is expected that a hypnotic with shorter drug duration will allow greater memory consolidation than a hypnotic with longer drug duration.


Study summary:

A growing body of evidence has demonstrated that sleep promotes memory consolidation in healthy individuals. However, little research has been conducted regarding the effect of hypnotics on sleep-dependent memory. One study found that zopiclone (7.5 mg), but not brotizolam (0.25 mg), impaired sleep-dependent memory consolidation in normal sleepers. Another study reported significant impairment of sleep-dependent memory on a motor task with triazolam (0.375 mg), but not with zolpidem immediate release (10 mg). These studies provide some evidence that sedative-hypnotic drugs may impair sleep-dependent memory consolidation, but further investigation is clearly needed in this area. Because hypnotics are commonly prescribed for insomnia, it is important to determine if there is a significant risk of impairment in sleep-dependent memory consolidation associated with these medications. Further, investigation of alternative doses and drug regimens upon memory consolidation appears warranted. The purpose of the current study is to determine the effect of two hypnotic medications on sleep-dependent memory consolidation in normal sleepers. Zolpidem extended release, which will be active for most of the sleep period when administered at bedtime, will be compared to zaleplon, which will be active for half of the sleep period when administered in the middle of the night. This comparison allows us to address the question of whether a few hours of drug-free sleep results in better memory consolidation than sleep with drug throughout the night.


Criteria:

Inclusion Criteria: - 18 to 50 years of age - no sleep complaints or problems - good sleep quality per questionnaire - sufficient time in bed each night Exclusion Criteria: - any clinically significant unstable medical condition - recent psychiatric disorder - prior diagnosis or symptoms of a sleep disorder - recent history of substance abuse - recent use of prescription hypnotic medication or over-the-counter sleep aid - recent use of psychotropic medication - history of adverse reaction to benzodiazepines - body mass index > 36 - currently pregnant or nursing - currently working rotating or night shift - consumption of > 700 mg per day of xanthine-containing food or beverages - consumption of > 14 units of alcohol per week - smoke > 1 pack of cigarettes per day, use of chewing tobacco more than 3 times per day, or unable to refrain from smoking or chewing without distress or discomfort while in the sleep laboratory


NCT ID:

NCT01159652


Primary Contact:

Principal Investigator
Janine M Hall-Porter, PhD
St Luke's Hospital


Backup Contact:

N/A


Location Contact:

Chesterfield, Missouri 63017
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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