A Safety Study of AQUAVAN® (Fospropofol Disodium) Injection for Sedation During Minor Surgical Procedures.
Public ClinicalTrials.gov record NCT00327392. 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 Open-Label, Single Arm Study to Assess the Safety of AQUAVAN® (Fospropofol Disodium) Injection for Minimal-to-Moderate Sedation in Patients Undergoing Minor Surgical Procedures
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
Very often patients receive medications 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. With respect to minimal-to-moderate procedural sedation for minor surgical procedures, a patient is first given a pain-relief medication (analgesic) and then a medication to help him/her relax and keep calm (sedative). AQUAVAN is a chemically modified form of propofol, a commonly-used sedative drug. AQUAVAN acts like a slow release version of propofol, and is being studied to see if it can safely keep patients calm and relaxed during their medical procedure and then allow for rapid and clear-headed recovery.
Study identification
- NCT ID
- NCT00327392
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 2, Phase 3
- Enrollment
- 123 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
- Apr 30, 2006
- Primary completion
- Not listed
- Completion
- Nov 30, 2007
- Last update posted
- Jun 19, 2012
2006 – 2007
United States locations
- U.S. sites
- 15
- U.S. states
- 12
- U.S. cities
- 14
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Precision Trials | Phoenix | Arizona | 85032 | — |
| Borland-Groover Clinic | Jacksonville | Florida | 32256 | — |
| University of Louisville | Louisville | Kentucky | 40202 | — |
| Medical Research Institute, Inc. | Slidell | Louisiana | 70458 | — |
| Medical Research Institute | Slidell | Louisiana | 70458 | — |
| Chevy Chase Clinical Research | Chevy Chase | Maryland | 20815 | — |
| Chesapeake Research Group, LLC | Pasadena | Maryland | 21122 | — |
| St. Louis Women's Healthcare Group | Chesterfield | Missouri | 63017 | — |
| International Heart Institute of Montana | Missoula | Montana | 59802 | — |
| Hudson Valley Urology, PC | Poughkeepsie | New York | 12601 | — |
| Duke University Medical Center | Durham | North Carolina | 27710 | — |
| Southern Orthopaedic Sports Medicine | Columbia | South Carolina | 29204 | — |
| Carolina Urologic Research | Myrtle Beach | South Carolina | 29572 | — |
| Dallas VA Medical Center | Dallas | Texas | 75216 | — |
| Physicians' Research Options | Sandy City | Utah | 84070 | — |
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 NCT00327392, 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 Jun 19, 2012 · Synced Sep 5, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT00327392 live on ClinicalTrials.gov.