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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01702272
Other study ID # DENVTS-US12-002
Secondary ID
Status Completed
Phase N/A
First received October 3, 2012
Last updated September 11, 2014
Start date January 2013
Est. completion date January 2014

Study information

Verified date September 2014
Source Gen-Probe, Incorporated
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Observational

Clinical Trial Summary

The objective of this study is to test individual donor samples (IDSs) with the investigational Dengue Assay on the TIGRIS System and to further characterize the Dengue Assay in the clinical setting.


Recruitment information / eligibility

Status Completed
Enrollment 150000
Est. completion date January 2014
Est. primary completion date January 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Donor must meet all the blood collection sites' standard eligibility requirements.

- Donor and/or legally authorized representative must be willing to undergo the site's routine informed consent process prior to study participation.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Device:
Procleix Dengue Virus Assay
in vitro diagnostic assay

Locations

Country Name City State
United States Creative Testing Solutions - Tampa St Petersburg Florida

Sponsors (1)

Lead Sponsor Collaborator
Gen-Probe, Incorporated

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Qualitative detection of ribosomal RNA from Dengue Virus in plasma specimens from individual human donors, including volunteer donors of whole blood and blood components, and other living donors. Approximately three years No
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