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Terminated Phase 3 Interventional Results available

To Compare Safety and Efficacy of Doripenem Versus Imipenem-Cilastatin in Patients With Ventilator-Associated Pneumonia

ClinicalTrials.gov ID: NCT00589693

Public ClinicalTrials.gov record NCT00589693. 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 Oct 27, 2026, 4:34 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 Prospective, Randomized, Double-Blind, Double-Dummy, Multicenter Study to Assess the Safety and Efficacy of Doripenem Compared With Imipenem-Cilastatin in the Treatment of Subjects With Ventilator-Associated Pneumonia

Brief summary

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

The purpose of this study is to show that doripenem is as effective as imipenem-cilastatin in the treatment of patients with ventilator-associated pneumonia.

Study identification

NCT ID
NCT00589693
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Enrollment
274 participants

Conditions and interventions

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 2008 (Type not available)
Primary completion
Jun 2011 (Actual)
Completion
Jun 2011 (Actual)
Last update posted
Dec 28, 2012

2008 – 2011

United States locations

U.S. sites
17
U.S. states
17
U.S. cities
17
Facility City State ZIP Site status
Not listed Jonesboro Arkansas — —
Not listed Newark Delaware — —
Not listed Washington D.C. District of Columbia — —
Not listed Jacksonville Florida — —
Not listed Moline Illinois — —
Not listed Hazard Kentucky — —
Not listed Biddeford Maine — —
Not listed Baltimore Maryland — —
Not listed Detroit Michigan — —
Not listed Butte Montana — —
Not listed Buffalo New York — —
Not listed Winston-Salem North Carolina — —
Not listed Cincinnati Ohio — —
Not listed Oklahoma City Oklahoma — —
Not listed Nashville Tennessee — —
Not listed Houston Texas — —
Not listed Milwaukee Wisconsin — —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 83 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00589693, 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 Dec 28, 2012 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00589693 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →