Clinical Trials Directory

Trials / Completed

CompletedNCT01662362

Abbott ESA Chagas Assay Post-Market Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
63 (actual)
Sponsor
Abbott Diagnostics Division · Industry
Sex
All
Age
17 Years
Healthy volunteers
Accepted

Summary

The study is conducted to meet an FDA post market commitment to collect and report data on the performance of the ESA Chagas assay. A minimum of 50 donor specimens that are FDA-licensed ABBOTT PRISM Chagas repeatedly reactive (RR)will be tested with the ABBOTT ESA Chagas assay. In addition, minimum of 300 ABBOTT PRISM Chagas nonreactive (NR) unidentified donor specimens will be tested with ABBOTT ESA Chagas assay.

Detailed description

ABBOTT ESA Chagas testing will be performed at a minimum of two blood donor centers. Testing will be performed using the FDA-licensed ESA Chagas assay and will be performed in accordance with the ESA Chagas package insert. ABBOTT PRISM Chagas repeatedly reactive blood donor specimens identified by U.S. blood donor centers, as part of the routine blood donation process, will be tested with the FDA-licensed ESA Chagas. Specimens will also be tested with radioimmune precipitation assay (RIPA) for antibody to T. cruzi, a laboratory developed test, and the FDA-licensed ORTHO T. cruzi ELISA. The donor centers will contact the donors and request the donor to return to complete a questionnaire and provide a follow-up specimen. In addition, a minimum of 300 blood donor specimens with ABBOTT PRISM Chagas nonreactive results will also be tested with ESA Chagas. These specimens will be unidentified, leftover specimens from routine donor testing and not individually identifiable. Specimens that are positive or indeterminate with ESA Chagas will be further tested with RIPA.

Conditions

Interventions

TypeNameDescription
DEVICETesting Donor Specimens with ESA ChagasDonors will be asked to return for a follow-up blood draw.

Timeline

Start date
2012-07-01
Primary completion
2012-12-01
Completion
2012-12-01
First posted
2012-08-10
Last updated
2014-02-20
Results posted
2014-02-20

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01662362. Inclusion in this directory is not an endorsement.