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NCT01919931 Clinical Trial

Immunological Interaction Between the Host and Candida Albicans Biofilm

Candidiasis Clinical Trial

Official title:
Immunological and Molecular Interaction Between the Host and Candida Albicans Biofilm

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01919931
Other study ID # S55012
Secondary ID
Status Completed
Phase N/A
First received June 19, 2013
Last updated December 6, 2016
Start date March 2013
Est. completion date January 2016

Study information
Verified date December 2016
Source Universitaire Ziekenhuizen Leuven
Contact n/a
Is FDA regulated No
Health authority Belgium: Institutional Review Board
Study type Observational

Clinical Trial Summary

Candida albicans is one of the most common nosocomial infection and the onset relies on the host immune status. The purpose of this study is to determine the immunological profile of patients infected with Candida albicans, that could ideally lead to a strategy to identify patients who could benefit from prophylaxis.

Recruitment information / eligibility
Status Completed
Enrollment 237
Est. completion date January 2016
Est. primary completion date August 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients infected with Candida albicans

- Patients not infected with Candida albicans

Exclusion Criteria:

- Underage patients

- Non consenting patients

- Unconscious patients

Study Design

Observational Model: Case Control, Time Perspective: Retrospective

Related Conditions & MeSH terms

Locations
Country Name City State
Belgium Universitair Ziekenhuis Leuven Leuven Flemish Brabant

Sponsors (1)
Lead Sponsor Collaborator
Universitaire Ziekenhuizen Leuven

Country where clinical trial is conducted

Belgium, 

Outcome
Type Measure Description Time frame Safety issue
Primary Immunological phenotyping of patients 2 months No
Secondary Mannose Binding Lectin levels 1 month No
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