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Trial · NCT00666939

A Study of Single-Dose Gabapentin in Subjects With Transient Insomnia Induced by a Sleep Phase Advance

NCT00666939, Phase 3, Completed, Pfizer's Upjohn has merged with Mylan to form Viatris Inc.

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. A Study of Single-Dose Gabapentin in Subjects With Transient Insomnia Induced by a Sleep Phase Advance. Trials, record NCT00666939. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00666939

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
A Study of Single-Dose Gabapentin in Subjects With Transient Insomnia Induced by a Sleep Phase Advance
NCT number
NCT00666939
Status
Completed
Phases
Phase 3
Enrollment
773 participants, actual
Lead sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
Conditions
Transient Insomnia
Interventions
Gabapentin, Gabapentin, Placebo
First posted
2008-04-25
Last updated
2021-02-02

Source ClinicalTrials.gov

Registered outcomes13

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimarySubjective sleep latencyHour +8
SecondaryStanford Sleepiness ScaleHour +13
SecondaryVital signsHour +8
SecondaryAdverse eventsHour +13
SecondarySubjective number of awakeningsHour +8
SecondarySubjective wake after sleep onsetHour +8
SecondarySubjective total sleep timeHour +8
SecondarySubjective assessment of sleep refreshmentHour +8
SecondarySubjective assessment of sleep qualityHour +8
SecondaryKarolinska Sleep Diary-Sleep (KSD) Quality IndexHour +8

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests2

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource
Selective Reminding TaskSecondary outcomeConductCognition
Symbol CodingSecondary outcomeConductCognition

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT00666939

GET https://conductscience.org/api/trials/v1/NCT00666939/registered