An Effectiveness and Safety Study of AQUAVAN® Injection (Fospropofol Disodium) for Sedation During Flexible Bronchoscopy
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.
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
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
Very often patients receive medication before a diagnostic, therapeutic, or surgical procedure to help them relax, keep them calm, and to relieve them from pain. This is called procedural sedation. During procedural (mild-to-moderate) sedation, a patient is first given a pain-relief medication (analgesic) and then a medication to help him/her relax and keep him/her calm (sedative). Propofol is the drug commonly used for sedation because it releases immediately into the blood stream and causes fast sedation. AQUAVAN (fospropofol disodium) is made as a slow release version of propofol with a longer duration of effect.
Study identification
- NCT ID
- NCT00306722
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 3
- Enrollment
- 250 participants
Conditions and interventions
Conditions
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 Sep 6, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT00306722 live on ClinicalTrials.gov.