Antimycotic Prophylaxis in Pediatric Patients Following Allogeneic Stem Cell Transplantation

NCT ID: NCT01040156

Last Updated: 2009-12-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Study Classification

OBSERVATIONAL

Study Start Date

2008-08-31

Study Completion Date

2009-12-31

Brief Summary

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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.

Detailed Description

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Conditions

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Systemic Aspergillosis Systemic Candidiasis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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LAmb

No interventions assigned to this group

Cas

No interventions assigned to this group

Eligibility Criteria

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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
Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Children's Hospital Tuebingen

OTHER

Sponsor Role lead

Principal Investigators

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Ingo Mueller, M.D.

Role: PRINCIPAL_INVESTIGATOR

UCHT

Locations

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University Children's Hospital

Tübingen, , Germany

Site Status

Countries

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Germany

Other Identifiers

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UCHT-1209

Identifier Type: -

Identifier Source: org_study_id