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NCT00463762 Clinical Trial

Cefoperazone/Sulbactam In The Treatment Of Serious Intra-Abdominal And Hepatobiliary Infections.

Appendicitis Clinical Trial

Official title:
Cefoperazone/Sulbactam In The Treatment Of Serious Intra-Abdominal And Hepatobiliary Infections In Slovakia. An Open, Prospective, Non-Comparative Study.

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT00463762
Other study ID # A1891004
Secondary ID
Status Withdrawn
Phase Phase 4
First received April 17, 2007
Last updated April 21, 2011
Start date May 2007

Study information
Verified date April 2011
Source Pfizer
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Observational

Clinical Trial Summary

The primary objective is to collect data on treatment outcomes (clinical and microbiological cure), safety and tolerability of treatment with cefoperazone/sulbactam in patients with serious intra-abdominal and hepatobiliary infections in Slovakia.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Male or female patient of age 18 years or older.

- Patient with intraabdominal/hepatobiliary infection.?

Exclusion Criteria:

- Patients with known hypersensitivity to penicillins, cephalosporins, cefoperazone or to sulbactam.

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Drug:
• CP-75385-02 Cefoperazone/sulbactam

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Pfizer
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