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Trial record 39 of 39 for:    FLUMAZENIL

Positron Emission Tomography Assessment of the Central Nervous System Effects of Eszopiclone and Zolpidem

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: NCT00781482
Recruitment Status : Withdrawn (Sponsor elected not to conduct study at this time.)
First Posted : October 29, 2008
Last Update Posted : February 26, 2016
Abiant, Inc.
Information provided by:
Kettering Health Network

Brief Summary:
This study will compare the interactions of a placebo and two FDA-approved sleeping medications, Eszopiclone (Lunesta) and Zolpidem (Ambien), with certain chemical receptors in the brain. We want to show that we can use positron emission tomography images to measure the binding of these medications to the receptors.

Condition or disease Intervention/treatment Phase
Healthy Drug: eszopiclone, zolpidem, placebo Phase 4

Detailed Description:

We will enroll 4 normal, healthy, adult male volunteers who will undergo screening tests (labs, EKGs, medical history, physical exam, and MRI of the brain) for safety. If eligible, they will return for three separate positron emission tomography (PET) scans. Over the course of the three study visits, each subject will receive eszopiclone (Lunesta), zolpidem (ambien) and a placebo in random order.

After each medication or placebo dose, a PET scan will be done using a [11-C] flumazenil (Romazicon). The flumazenil will help us measure the binding of the study medications to chemical receptors called GABA receptors in certain parts of the brain.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 0 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Basic Science
Official Title: Positron Emission Tomography Assessment of the Central Nervous System Effects of Eszopiclone and Zolpidem

Resource links provided by the National Library of Medicine

Arm Intervention/treatment
Experimental: 1
This is a crossover study. Each study drug will be administered (one at a time and in random order) to each subject on separate occasions over the course of the study.
Drug: eszopiclone, zolpidem, placebo
In random order, each subject will receive one study drug per visit over three visits. Visits will occur about 1 week apart. Each subject will eventually receive eszopiclone 3 mg., zolpidem 10 mg., and a placebo. PET scans will be done 1-2 hours after each dose.
Other Names:
  • Lunesta
  • Ambien

Primary Outcome Measures :
  1. We will measure GABA receptor binding by PET imageing after each dose of study medication or placebo. [ Time Frame: PET scans will occur within 1-2 hours after study drug or placebo administration. Visits will occur approximately 1 week apart. . Subjects will have visits scheduled over approximately 6 weeks, including screening, scanning visits, and follow-up. ]

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 35 Years   (Adult)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Healthy Males age 18 to 35 inclusive
  • Body Mass Index 18 to 30
  • Willing to adhere to prohibitions and restrictions specified in protocol
  • Must give informed consent.

Exclusion Criteria:

  • Clinically significant abnormal lab values for chemistry, hematology or urinalysis at screening.
  • Clinically significant abnormal physical exam, vital signs, or 12-lead EKG at screening
  • Significant history of or current significant medical illness.
  • Significant history of or current psychiatric or neurological illness or sleep apnea.
  • Participation in another research study involving exposure to ionizing radiation within the last 12 months.
  • Any clinically significant MR abnormality which may be relevant to the study.
  • Metal implants which are relevant for MR or PET procedures or data.
  • History of epilepsy or fits or unexplained blackouts.
  • Serology positive for Hepatitis B surface antigen, Hepatitis C antibodies, or HIV antibodies.
  • Positive urine screen for drugs of abuse.
  • Positive alcohol screen.
  • Known or suspected alcoholism or drug addiction even if currently abstaining
  • Drinks on average more than 8 cups of coffee, tea, cocoa, or cola per day.
  • Smoking cigarettes within 3 months prior to study drug administration.
  • Clinically significant acute illnes within 7 days of study drug administration.
  • Claustrophobia.
  • Donation of 1 or more units of blood (approximately 450ml), or acute loss of an equivalent amount of blood within 90 days prior to study drug administration.
  • Have received an experimental drug or used an experimental medical device within 90 days of planned start of treatment with drugs for this study.
  • Use of any prescription or over the counter medication, or herbal medication (not including non-steroidal anti-inflammatory drugs) within 2 weeks of the first PET scan. Of particular concern would be GABA-ergic compounds and CYP3A4 inhibitors. Exclusion should also be considered if the subject has taken a drug with a long half-life (or of any metabolite) even if taken outside the two week time window. However, the subject can still be enrolled if, in the opinion of the investigator, such medication taken in that timeframe will not interfere with the results of the study.
  • Psychological or emotional problems that would render the informed consent invalid or limit the ability of the subject to comply with the study requirements.
  • Any condition that in the opinion of the investigator would complicate or compromise the study, or the well-being of the subject.

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): NCT00781482

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United States, Ohio
Kettering Medical Center
Kettering, Ohio, United States, 45429
Sponsors and Collaborators
Kettering Health Network
Abiant, Inc.
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Principal Investigator: Joseph C Mantil, MD, PhD Kettering Health Network

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Responsible Party: Joseph Mantil, MD, PhD, Kettering Health Network Identifier: NCT00781482     History of Changes
Other Study ID Numbers: 07-104-SEPR
First Posted: October 29, 2008    Key Record Dates
Last Update Posted: February 26, 2016
Last Verified: February 2016
Keywords provided by Kettering Health Network:
Positron Emission Tomography
GABA receptor binding
Hypnotic Drugs
[11-C] Flumazenil
Molecular imaging of the brain
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