Trials / Completed
CompletedNCT00388167
Acetato de Caspofungin (Cancidas®) in the Treatment of Fungal Infection
PROCAS: Study Observational Prospective and Multicenter to Determine the Clinic Effectiveness and the Safety of Caspofungin Acetate (CANCIDAS®) in the Treatment of Invader Fungal Infection
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 320 (estimated)
- Sponsor
- PETHEMA Foundation · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
We wanted to determine the efficacy and the safety of caspofungin acetate (CANCIDAS®) in the treatment of invader fungal infection (IFI) specifically, Invasive Candidiasis (CI) in adults patients without neutropenia and Invasive Aspergillosis (AI) in adults patients who are refractory to or intolerant of other therapies (i.e., amphotericin B, lipid formulations of amphotericin B, and/or itraconazole).
Detailed description
Study post-marketing (observational). It is multicenter and prospective. No masking is used, without control group neither is randomized
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Caspofungin | The patients are treated with 70 mg IV of caspofungin on day 1, followed by 50 mg/day IV during the rest of treatment |
Timeline
- Start date
- 2004-03-01
- Completion
- 2008-02-01
- First posted
- 2006-10-16
- Last updated
- 2009-05-13
Locations
27 sites across 1 country: Spain
Source: ClinicalTrials.gov record NCT00388167. Inclusion in this directory is not an endorsement.