Viewing Study NCT00300534



Ignite Creation Date: 2024-05-05 @ 4:45 PM
Last Modification Date: 2024-10-26 @ 9:23 AM
Study NCT ID: NCT00300534
Status: COMPLETED
Last Update Posted: 2012-09-07
First Post: 2006-03-02

Brief Title: Multi-site Study of Rapid Diagnostic Syphilis Assays
Sponsor: Centers for Disease Control and Prevention
Organization: Centers for Disease Control and Prevention

Study Overview

Official Title: Multi-site Study of Rapid Diagnostic Syphilis Assays of Persons Attending STD Clinics in High Syphilis Morbidity Areas
Status: COMPLETED
Status Verified Date: 2012-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The performance of an investigational immunochromatographic strip ICS test for the diagnosis of syphilis is compared with the Abbott Laboratories Determine ICS test The study population consists of patients with and without syphilis presenting to sexually transmitted disease clinics in five cities in the United States Specimens include finger-stick whole blood investigational test only and whole blood plasma and serum by venipuncture
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None