ClinicalTrials.gov record
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 May 8, 2026, 12:28 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

Study identification

NCT ID
NCT00080496
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Industry
Enrollment
430 participants

Conditions and interventions

Interventions

  • Cilastatin Drug
  • Imipenem Drug
  • Tigecycline Drug

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
Jun 30, 2003
Primary completion
Not listed
Completion
Nov 30, 2006
Last update posted
Aug 3, 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 3, 2008 · Synced May 8, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00080496 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →