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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00445094
Other study ID # 0787B-092
Secondary ID 2007_004
Status Completed
Phase Phase 4
First received March 6, 2007
Last updated February 15, 2017
Start date November 2006
Est. completion date January 2007

Study information

Verified date February 2017
Source Merck Sharp & Dohme Corp.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary objective of this study is a comparison between MK0787B and standard therapy.


Recruitment information / eligibility

Status Completed
Enrollment 120
Est. completion date January 2007
Est. primary completion date January 2007
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Greater than 18 years of age

- Patient is diagnosed with nosocomial pneumonia

Exclusion Criteria:

- Immunological deficient patients

- Pregnant women and nursing mothers

- A fungus is identified before the study enrollment

- Received vancomycin or imipenem for more than 5 days before icu admission

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
MK0787B, imipenem/cilastatin sodium / Duration of Treatment: 7 Days

Comparator: amikacin / Duration of Treatment: 3 Days

Comparator: tazocin / Duration of Treatment: 3 Days

Comparator: vancomycin / Duration of Treatment: 3 Days


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Merck Sharp & Dohme Corp.

Outcome

Type Measure Description Time frame Safety issue
Primary A 30-day-survival rate in the intensive care unit evaluated by Acute Physiology and Chronic Health (APACH II) Disease Classification System II score
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