Point of Care Testing for Presence of Current and or Previous T. Gondii Infection

Recruiting N/A Interventional Study
Toxoplasma Infections
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 – 90
Sex
Any
Study type
Interventional
Purpose
Diagnostic
Participants needed
210 (estimated)
Sponsor
University of Chicago · Other
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About This Trial
This is part of a feasibility study to compare the predicate standard FDA cleared test for serum to a point of care test Toxoplasma ICT IgG-IgM BK produced by LD Bio Diagnostic. The specificity and sensitivity in testing serum and whole blood will be compared. This study includes 70 persons either pregnant or non pregnant. This is being done in accordance with FDA requirements for clearance of a …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * any adult who is willing to participate in the study Exclusion Criteria: * pregnant women who are in their 17-27 weeks of gestation.
Contacts

Rima McLeod, M.D.

312-513-6365

rmcleod@uchicago.edu

CONTACT

Marcela Cid

714-376-4412

mcidrosas@uchicago.edu

CONTACT