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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01207843
Other study ID # idr-3d-001
Secondary ID
Status Completed
Phase Phase 4
First received September 21, 2010
Last updated August 18, 2014
Start date October 2009
Est. completion date May 2013

Study information

Verified date August 2014
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Observational

Clinical Trial Summary

Hepatic candidiasis is a frequent complication in patients receiving intensive chemotherapy for acute leukemia. Hepatic lesions may be detected by computerized tomographic (CT) scans, but there is no standardized CT protocol for the diagnosis and follow-up of hepatic candidiasis.

The investigators compared the size of the fungal lesions in the chest and abdomen CT. The current analysis aimed to increase the value of CT for the diagnosis and the follow-up of hepatic candidiasis in daily routine.


Recruitment information / eligibility

Status Completed
Enrollment 88
Est. completion date May 2013
Est. primary completion date April 2011
Accepts healthy volunteers No
Gender Both
Age group 16 Years to 80 Years
Eligibility Inclusion criteria:

- Chest and Abdomen CT with fungal lesion in patients with leukemia

Exclusion criteria:

- Other liver pathologies

Study Design

Time Perspective: Retrospective


Related Conditions & MeSH terms


Intervention

Behavioral:
Imaging
CT image validation and lesion measurement, as well as comparison of different CT phases

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary The primary end-point was IFI according to the EORTC/MSG 2008 definitions and bacteraemia 2 Years No
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