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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01040156
Other study ID # UCHT-1209
Secondary ID
Status Completed
Phase N/A
First received December 28, 2009
Last updated December 28, 2009
Start date August 2008
Est. completion date December 2009

Study information

Verified date December 2009
Source University Children’s Hospital Tuebingen
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Observational

Clinical Trial Summary

Pediatric patients are at high risk to acquire mycotic infections following allogeneic bone marrow transplantation. In the present retrospective analysis we assess the safety and efficacy of different regimens in antimycotic prophylaxis.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date December 2009
Est. primary completion date December 2009
Accepts healthy volunteers
Gender Both
Age group N/A to 18 Years
Eligibility Inclusion Criteria:

- Pediatric patients under the age of 18 years

- Pediatric patients after HSCT treated with caspofungin

- Pediatric patients after HSCT treated with liposomal amphotericin

Exclusion Criteria:

- Pediatric patients with uncontrolled hematological malignancies

- Pediatric patients with IFI at start of HSCT

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Locations

Country Name City State
Germany University Children's Hospital Tuebingen

Sponsors (1)

Lead Sponsor Collaborator
University Children’s Hospital Tuebingen

Country where clinical trial is conducted

Germany,