ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Study of the Efficacy and Multiple-Dose Plasma Concentration-Time Profiles of Armodafinil and PROVIGIL

ClinicalTrials.gov ID: NCT00236080

Public ClinicalTrials.gov record NCT00236080. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 8, 2026, 8:10 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study of the Efficacy and Multiple-Dose Plasma Concentration-Time Profiles of Armodafinil (150, 200, and 250 mg) and PROVIGIL® (200 mg) in Patients With Chronic Shift Work Sleep Disorder

Study identification

NCT ID
NCT00236080
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Cephalon
Industry
Enrollment
136 participants

Conditions and interventions

Interventions

  • Armodafinil 150 mg Drug
  • Armodafinil 200 mg Drug
  • Armodafinil 250 mg Drug
  • PROVIGIL 200 mg Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 31, 2005
Primary completion
Not listed
Completion
Nov 30, 2005
Last update posted
Jul 18, 2013

2005

United States locations

U.S. sites
20
U.S. states
15
U.S. cities
19
Facility City State ZIP Site status
Psypharma Clinical Research Phoenix Arizona 85050
PsyPharma Clinical Tucson Tucson Arizona 85712
Central Arkansas Research Hot Springs Arkansas 71913
Pacific Sleep Medicine Service Los Angeles California 90048
Pacific Sleep Medicine Service San Diego California 92121
BMR HealthQuest San Diego California 92123
Stanford University Stanford California 94305
Neurotrials Research Atlanta Georgia 30342
SLEEPMED, Inc. Macon Georgia 31202
Henry Lahmeyer, MD Northfield Illinois 60093
Vince and Associates Clinical Overland Park Kansas 66211
Center for Sleep/Wake Disorder Chevy Chase Maryland 20815
Brigham and Women's Hospital Boston Massachusetts 02115
Clinical Rsch Center of Nevada Las Vegas Nevada 89104
Clinilabs / Sleep Disorders In New York New York 10025
Wake Research Associates Raleigh North Carolina 27612
St. Vincent Mercy Medical Cent Toledo Ohio 43608
Consolidated Clinical Trials Pittsburgh Pennsylvania 15221
SleepMed of South Carolina Columbia South Carolina 29201
Radiant Research Salt Lake Salt Lake City Utah 84107

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00236080, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 18, 2013 · Synced May 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00236080 live on ClinicalTrials.gov.

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