Immunological Interaction Between the Host and Candida Albicans Biofilm
Sponsor
Universitaire Ziekenhuizen Leuven (Other)
Overall Status
Completed
CT.gov ID
NCT01919931
Collaborator
(none)
237
1
34
7
Study Details
Study Description
Brief 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.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Study Design
Study Type:
Observational
Actual Enrollment
:
237 participants
Observational Model:
Case-Control
Time Perspective:
Retrospective
Official Title:
Immunological and Molecular Interaction Between the Host and Candida Albicans Biofilm
Study Start Date
:
Mar 1, 2013
Actual Primary Completion Date
:
Aug 1, 2015
Actual Study Completion Date
:
Jan 1, 2016
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
Candida Infection Patients infected with Candida albicans |
|
No infection Patients with no Candida albicans infection |
Outcome Measures
Primary Outcome Measures
- Immunological phenotyping of patients [2 months]
Secondary Outcome Measures
- Mannose Binding Lectin levels [1 month]
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
-
Patients infected with Candida albicans
-
Patients not infected with Candida albicans
Exclusion Criteria:
-
Underage patients
-
Non consenting patients
-
Unconscious patients
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Universitair Ziekenhuis Leuven | Leuven | Flemish Brabant | Belgium | 3000 |
Sponsors and Collaborators
- Universitaire Ziekenhuizen Leuven
Investigators
- Study Director: Adrian Liston, Group Leader, Flemish Institute of Biotechnology
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Universitaire Ziekenhuizen Leuven
ClinicalTrials.gov Identifier:
NCT01919931
Other Study ID Numbers:
- S55012
First Posted:
Aug 9, 2013
Last Update Posted:
Dec 7, 2016
Last Verified:
Dec 1, 2016
Keywords provided by Universitaire Ziekenhuizen Leuven
Additional relevant MeSH terms: