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NCT00167375 · ClinicalTrials.gov registry record

Testing the Nocturnal Sleep Latency Profile in Primary Insomnia

A clinical trial of Sleep Initiation and Maintenance Disorders and Primary Insomnia, sponsored by University of Pittsburgh.

Completed
Registry status
24
Enrollment target
1
Study location

NCT00167375 is a study of Sleep Initiation and Maintenance Disorders and Primary Insomnia that has completed, run by University of Pittsburgh. The registered enrollment target is 24 participants, below the 289-participant average among 19 other Sleep Initiation and Maintenance Disorders trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00167375, a study of Sleep Initiation and Maintenance Disorders and Primary Insomnia, has completed, sponsored by University of Pittsburgh.

COMPLETED
Registry status
24 participants
Enrollment target
1
Study location

Study Summary

This study tests a new kind of sleep study in which subjects are awakened 2 times after initially going to sleep. The study focuses on the EEG signal process as a person goes to sleep. The general hypothesis is that the signal properties are stable from night to night during baseline studies, and are different between controls and patients with primary insomnia. The primary insomnia patients then go on to have about 2 weeks of an insomnia intervention. Then the new kind of study is repeated in the patients. The controls only are examined in baseline studies.

Interventions

  • DRUG eszopiclone 3 mg qHS
  • BEHAVIORAL General cognitive/behavioral interventions for insomnia

Study Locations (1)

Pennsylvania

  • Western Psychiatric Institute and Clinic - Pittsburgh

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2005-01
Est. Completion 2007-06

Sponsor

University of Pittsburgh

1,238 total trials

What the Registry Record Tells You About NCT00167375

The ClinicalTrials.gov registry entry for NCT00167375 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 24 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 289-participant average among 19 other Sleep Initiation and Maintenance Disorders trials with a reported enrollment target (92% lower). The listed sponsor is University of Pittsburgh, which has 1,238 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Sleep Initiation and Maintenance Disorders appearing as the primary indexed condition, and to 2 interventions - of which eszopiclone 3 mg qHS is the first listed.

NCT00167375 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT00167375 about?

NCT00167375 is a clinical study titled "Testing the Nocturnal Sleep Latency Profile in Primary Insomnia". This study tests a new kind of sleep study in which subjects are awakened 2 times after initially going to sleep. The study focuses on the EEG signal process as a person goes to sleep. The general hypothesis is that the signal properties are stable from night to night during baseline studies, and ar...

What is the current status of trial NCT00167375?

This trial is currently completed. The enrollment target is 24 participants. The study started on 2005-01. Estimated completion is 2007-06.

What conditions does trial NCT00167375 study?

This clinical trial studies the following conditions: Sleep Initiation and Maintenance Disorders, Primary Insomnia.

What interventions are being tested in trial NCT00167375?

The interventions under investigation include: eszopiclone 3 mg qHS (DRUG), General cognitive/behavioral interventions for insomnia (BEHAVIORAL).

Who is sponsoring clinical trial NCT00167375?

This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00167375 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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