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Completed Phase 3 Interventional

An Effectiveness and Safety Study of AQUAVAN® Injection (Fospropofol Disodium) for Sedation During Flexible Bronchoscopy

ClinicalTrials.gov ID: NCT00306722

Public ClinicalTrials.gov record NCT00306722. 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 Jul 21, 2026, 2:17 PM 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 Phase 3, Randomized, Double-Blind, Dose-Controlled Study To Assess The Efficacy And Safety Of AQUAVAN® (Fospropofol Disodium) Injection For Minimal-To-Moderate Sedation In Patients Undergoing Flexible Bronchoscopy

Study identification

NCT ID
NCT00306722
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Eisai Inc.
Industry
Enrollment
250 participants

Conditions and interventions

Interventions

  • AQUAVAN® (fospropofol disodium) Injection Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Mar 31, 2006
Primary completion
Not listed
Completion
Apr 30, 2007
Last update posted
Nov 6, 2008

2006 – 2007

United States locations

U.S. sites
25
U.S. states
17
U.S. cities
23
Facility City State ZIP Site status
Pulmonary Associates of Mobile, PC Mobile Alabama 36608
Precision Trials Phoenix Arizona 85032
Saddleback Memorial Medical Center Laguna Hills California 92653
USC Health Science Campus (USC University Hospital) Los Angeles California 90033
Pensacola Research Consultants, Inc. Pensacola Florida 32503
Acute Care Consultants Inc. Augusta Georgia 30909
Graves-Gilbert Clinic Bowling Green Kentucky 42101
Central Maine Pulmonary Associates Auburn Maine 04210
Berkshire Medical Center Pittsfield Maryland 01201
Hurley Medical Center Flint Michigan 48503
Keith Popovich, MD, PLLC Butte Montana 59701
International Heart Institue of MT Foundation Missoula Montana 59802
University of Nebraska Medical Center Omaha Nebraska 68198
United Health Scrvices Hosptial, INC Johnson City New York 13790
Brody School of Medicine Greenville North Carolina 27834
ALL-TRIALS Clinical Research, LLC Winston-Salem North Carolina 27103
University of Cincinnati, The University Hospital Cincinnati Ohio 45267
Lowcountry Lung & Critical Care, PA Charleston South Carolina 29406
Medical University of South Carolina Charleston South Carolina 29425
Greenville Hospital System Greenville South Carolina 29605
South Carolina Pharmaceutical Research Spartanburg South Carolina 29303
Spartanburg Medical Research Spartanburg South Carolina 29303
The University of Texas Medical Branch Division of APICS Galveston Texas 77555
Johnston Memorial Hospital Pulmonary Research Abingdon Virginia 24210
Pulmonary Associates of Fredericksburg, Inc. Fredericksburg Virginia 22401

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 NCT00306722, 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 Nov 6, 2008 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00306722 live on ClinicalTrials.gov.

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