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NCT00666770 · ClinicalTrials.gov registry record · Phase 3
A Polysomnographic Study of Single-Dose Gabapentin in Transient Insomnia Induced by a Sleep Phase Advance
A Phase 3 study of Transient Insomnia, sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris.
- Completed
- Registry status
- Phase 3
- Development phase
- 309
- Enrollment target
- 5
- Study locations
NCT00666770 is a Phase 3 study of Transient Insomnia that has completed, run by Pfizer's Upjohn has merged with Mylan to form Viatris. The registered enrollment target is 309 participants. The trial reports 5 study locations across 3 states.
The verdict
NCT00666770, a Phase 3 study of Transient Insomnia, has completed, sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 309 participants
- Enrollment target
- 5
- Study locations
Study Summary
The purpose of this study is to assess the effect of gabapentin as compared to placebo on sleep in subjects with transient insomnia.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Gabapentin
Study Locations (5)
California
- Pfizer Investigational Site - Glendale
- Pfizer Investigational Site - San Diego
Kansas
- Pfizer Investigational Site - Overland Park
- Pfizer Investigational Site - Overland Park
New York
- Pfizer Investigational Site - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 309 participants |
| Start Date | 2004-10 |
| Est. Completion | 2004-11 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00666770
The ClinicalTrials.gov registry entry for NCT00666770 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 309 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer's Upjohn has merged with Mylan to form Viatris, which has 158 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Transient Insomnia appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.
NCT00666770 reports 5 study locations spanning 3 distinct geographic areas - top geographies include California, Kansas, New York.
Frequently Asked Questions
What is clinical trial NCT00666770 about?
NCT00666770 is a clinical study titled "A Polysomnographic Study of Single-Dose Gabapentin in Transient Insomnia Induced by a Sleep Phase Advance". The purpose of this study is to assess the effect of gabapentin as compared to placebo on sleep in subjects with transient insomnia.
What is the current status of trial NCT00666770?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 309 participants. The study started on 2004-10. Estimated completion is 2004-11.
What conditions does trial NCT00666770 study?
This clinical trial studies the following conditions: Transient Insomnia.
What interventions are being tested in trial NCT00666770?
The interventions under investigation include: Placebo (DRUG), Gabapentin (DRUG).
Who is sponsoring clinical trial NCT00666770?
This trial is sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris, which has 158 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00666770 being conducted?
This trial has 5 study locations across California, Kansas, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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