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Completed Phase 3 Interventional

Study of Clevidipine Assessing Its Postoperative Antihypertensive Effect in Cardiac Surgery (ESCAPE-2)

ClinicalTrials.gov ID: NCT00093262

Public ClinicalTrials.gov record NCT00093262. 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 Sep 2, 2026, 1:40 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

Efficacy Study of Clevidipine Assessing Its Postoperative Antihypertensive Effect in Cardiac Surgery (ESCAPE-2)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to establish the efficacy of of clevidipine versus placebo in treating postoperative hypertension. Approximately 100 patients with postoperative hypertension undergoing coronary artery bypass grafting (CABG), off-pump coronary artery bypass (OPCAB) or minimally invasive direct coronary artery bypass (MIDCAB) surgery and/or valve replacement/repair procedures were anticipated to be randomly assigned to one of two treatment groups: clevidipine or placebo.

Study identification

NCT ID
NCT00093262
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
The Medicines Company
Industry
Enrollment
206 participants

Conditions and interventions

Conditions

Interventions

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
Nov 30, 2003
Primary completion
Sep 30, 2004
Completion
Sep 30, 2004
Last update posted
May 7, 2014

2003 – 2004

United States locations

U.S. sites
15
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
Discovery Alliance - Mobile Infirmary Medical Center Mobile Alabama 36602
Keck School of Medicine, University of Southern California Los Angeles California 90033
Huntington Memorial Hospital Pasadena California 91109
Stanford University School of Medicine Stanford California 94305-5640
Emory Hospital Atlanta Georgia 30322
Heart Care Research Foundation Blue Island Illinois 60406
MacNeal Hospital Glencoe Illinois 60022
Wesley Medical Center Wichita Kansas 67214
St. Lukes Hospital Kansas City Missouri 64111
International Heart Institute Missoula Montana 59802
Mt. Sinai Medical Center New York New York 10029-6574
Columbia University - College of Physicians and Surgeons New York New York 10032
Carolinas Medical Center Charlotte North Carolina 28203
Discovery Alliance - Methodist Hospital / Diagnostic West Pavillion Houston Texas 77030
Medical College of Wisconsin VAMC - Milwaukee Milwaukee Wisconsin 53295

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 NCT00093262, 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 May 7, 2014 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00093262 live on ClinicalTrials.gov.

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