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Completed Phase 3 Interventional

Study Evaluating Tigecycline Versus Imipenem/Cilastatin in Hospital-Acquired Pneumonia

ClinicalTrials.gov ID: NCT00080496

Public ClinicalTrials.gov record NCT00080496. 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 23, 2026, 7:10 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

A Phase 3, Multicenter, Randomized, Double-Blind, Comparative Study Of The Efficacy And Safety Of Tigecycline Vs Imipenem/Cilastatin For The Treatment Of Subjects With Nosocomial Pneumonia

Brief summary

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

To compare the efficacy and safety of the tigecycline regimen with that of the imipenem/cilastatin regimen in subjects with nosocomial pneumonia.

Study identification

NCT ID
NCT00080496
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
430 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 70 Years
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
Jul 2003 (Type not available)
Primary completion
Not listed
Completion
Dec 2006 (Actual)
Last update posted
Aug 4, 2008

2003 – 2006

United States locations

U.S. sites
29
U.S. states
13
U.S. cities
24
Facility City State ZIP Site status
Not listed Phoenix Arizona 85006 —
Not listed Phoenix Arizona 85013 —
Not listed Scottsdale Arizona 85251-6403 —
Not listed Scottsdale Arizona 85260-6709 —
Not listed Martinez California 94553 —
Not listed Modesto California 95350 —
Not listed Modesto California 95355 —
Not listed National City California 91950 —
Not listed Bay Pines Florida 33744 —
Not listed Crystal River Florida 34428 —
Not listed Gainesville Florida 32601 —
Not listed Orlando Florida 32806 —
Not listed Atlanta Georgia 30342 —
Not listed Augusta Georgia 30909 —
Not listed Roswell Georgia 30076 —
Not listed Chicago Illinois 60610 —
Not listed Springfield Illinois 62769 —
Not listed Springfield Illinois 62781 —
Not listed New Orleans Louisiana 70112 —
Not listed Shreveport Louisiana 71103 —
Not listed Baltimore Maryland 21201 —
Not listed Columbia Missouri 65212 —
Not listed Omaha Nebraska 68198-5300 —
Not listed Henderson North Carolina 27536 —
Not listed Cincinnati Ohio 45219 —
Not listed Zanesville Ohio 43071 —
Not listed Philadelphia Pennsylvania 19102 —
Not listed Philadelphia Pennsylvania 19140 —
Not listed Greenville South Carolina 29605 —

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 NCT00080496, 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 Aug 4, 2008 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00080496 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →