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Efficacy of Anidulafungin in the treatment of invasie candida infections in clinical practice

Conditions
invasive Candidiasis infection
B37
Candidiasis
Registration Number
DRKS00000074
Lead Sponsor
niversitätsklinik Freiburg
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
37
Inclusion Criteria

invasive mycosis through candida species

Exclusion Criteria

Treatment is compliant with approval of Anidulafungin.

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
- ongoing (< 7 days) improvement with regard to underlying disease after donation of Anidulafungin<br>- two negative blood analysis (3-7 days after start with therapy with Anidulafungin, samples to be collected with intervall of 24 h) in case of candidae or no evidence or agent persistence after end of therapy<br>- no necissity to change of antimykotic therapy after within 7 days of start after Anidulafungin treatment<br>
Secondary Outcome Measures
NameTimeMethod
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