Clinical Trials Directory

Trials / Completed

CompletedNCT00481962

Health Economic Assessment of Tygacil® in the Treatment of Secondary Peritonitis in Intensive Care Units (ICUs)

Health Economic Assessment of Tygacil® in the Treatment of Secondary Peritonitis in Intensive Care Units

Status
Completed
Phase
Study type
Observational
Enrollment
180 (actual)
Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The main goals of the study are: Assessment of Tygacil's cost-effectiveness; Process cost analysis from a hospital perspective (including length of stay, treatment costs, side effect management costs, costs of monitoring, costs of diagnostic procedures, cost of care (TISS 10 score etc.); Efficacy of Tygacil under usual care conditions (cure rate).

Conditions

Interventions

TypeNameDescription
DRUGTygacilInitial dose of 100mg followed by 50mg every 12 hours for 5 to 14 days

Timeline

Start date
2006-02-01
Primary completion
2008-12-01
Completion
2008-12-01
First posted
2007-06-04
Last updated
2009-09-28

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT00481962. Inclusion in this directory is not an endorsement.