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Trial record 48 of 136 for:    ZOLPIDEM

Effect Of Treatment With Oral Zolpidem On Polysomnography And Actigraphy Measures In Healthy Volunteers

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00716521
Recruitment Status : Completed
First Posted : July 16, 2008
Last Update Posted : April 24, 2009
Information provided by:

Brief Summary:
This study will assess the feasibility of conducting sleep studies in a clinical research unit environment. In addition, the sensitivity of polysomnography and mobile actigraphy technologies will be compared for evaluating sleep stages and sleep architecture.

Condition or disease Intervention/treatment Phase
Methodology Study Drug: placebo Drug: zolpidem Phase 1

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 11 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Single (Participant)
Primary Purpose: Basic Science
Official Title: Subject- And Investigator-Blinded, Sponsor-Open, Randomized, Single-Dose, Placebo-Controlled, 3-Way Crossover Study To Study Effect Of Treatment With Oral Zolpidem On Polysomnography And Actigraphy Measures In Healthy Volunteers
Study Start Date : July 2008
Actual Primary Completion Date : October 2008
Actual Study Completion Date : October 2008

Resource links provided by the National Library of Medicine

Arm Intervention/treatment
Placebo Comparator: Placebo
groups of 3-4 subjects for overnight polysomnography assessments
Drug: placebo
single oral dose placebo

Experimental: Low dose Zolpidem Drug: zolpidem
single oral dose, 5 mg zolpidem

Experimental: High dose zolpidem Drug: zolpidem
single oral dose, 10 mg zolpidem

Primary Outcome Measures :
  1. onset to persistent sleep [ Time Frame: minutes ]

Secondary Outcome Measures :
  1. awakenings after sleep onset [ Time Frame: minutes ]

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 55 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Age 18-55
  • BMI 18-30 kg/m2
  • body weight > 50 kg

Exclusion Criteria:

  • no history of sleep disorder
  • no concurrent medications
  • no alcohol use
  • no medical issues
  • no smoking

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00716521

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United States, Connecticut
Pfizer Investigational Site
New Haven, Connecticut, United States, 06511
Sponsors and Collaborators
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Study Director: Pfizer Call Center Pfizer
Additional Information:
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Responsible Party: Director, Clinical Trial Disclosure Group, Pfizer, Inc. Identifier: NCT00716521    
Other Study ID Numbers: A9001390
First Posted: July 16, 2008    Key Record Dates
Last Update Posted: April 24, 2009
Last Verified: April 2009
Keywords provided by Pfizer:
mobile actigraphy inpatient polysomnography actigraphy ambien
Additional relevant MeSH terms:
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Sleep Aids, Pharmaceutical
Hypnotics and Sedatives
Central Nervous System Depressants
Physiological Effects of Drugs
GABA-A Receptor Agonists
GABA Agonists
GABA Agents
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action