Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00900159 · ClinicalTrials.gov registry record · NA

Effects of Daytime Eszopiclone Administration in Shift Workers

A NA study, sponsored by Brigham and Women's Hospital.

Completed
Registry status
NA
Development phase
24
Enrollment target

NCT00900159: Completed NA study, sponsored by Brigham and Women's Hospital.

NCT00900159 is a NA study that has completed, run by Brigham and Women's Hospital. The registered enrollment target is 24 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00900159, a NA study, has completed, sponsored by Brigham and Women's Hospital.

COMPLETED
Registry status
NA
Development phase
24 participants
Enrollment target

Study Summary

The purpose of this study is to test the effects of eszopiclone on daytime sleep and overnight wakefulness in shift workers.

Primary Outcome

Participants underwent four Maintenance of Wakefulness Tests (MWT) at 2-hour intervals during the simulated night shift starting 5 hours after wake time. MWT range from 0 to 40 minutes, where shorter times to fall asleep represent greater sleepiness (worse). MWT tests are averaged, for a mean in minutes.

Interventions

  • DRUG matching placebo
  • DRUG eszopiclone

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2009-05
Est. Completion 2010-02
Phase NA
Brigham and Women's Hospital

937 total trials

What the finished NCT00900159 record still lists

NCT00900159 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 2 interventions - of which matching placebo is the first listed.

NCT00900159 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00900159 about?

NCT00900159 is a clinical study titled "Effects of Daytime Eszopiclone Administration in Shift Workers". The purpose of this study is to test the effects of eszopiclone on daytime sleep and overnight wakefulness in shift workers.

What is the current status of trial NCT00900159?

This trial is currently completed. It is a NA study. The enrollment target is 24 participants. The study started on 2009-05. Estimated completion is 2010-02.

What interventions are being tested in trial NCT00900159?

The interventions under investigation include: matching placebo (DRUG), eszopiclone (DRUG).

Who is sponsoring clinical trial NCT00900159?

This trial is sponsored by Brigham and Women's Hospital, which has 937 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00900159's enrollment target sits among peer trials

24 1736th of 2000 higher than 246 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02331979 · 24 participants · NA

    Improving Bladder Function in SCI by Neuromodulation

  • NCT03096197 · 24 participants · NA

    Exoskeleton and Spinal Cord Stimulation for SCI

  • NCT03223922 · 24 participants · NA

    Neurocognitive Functioning With Genu-Sparing Whole Brain Radiation Therapy for Brain Metastases

  • NCT03326921 · 24 participants · Phase 1

    HA-1 T TCR T Cell Immunotherapy for the Treatment of Patients With Relapsed or Refractory Acute Leukemia After Donor Stem Cell Transplant

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00900159, the US trial registry maintained by the National Library of Medicine. NCT00900159 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.