Evaluation of the MBio Combined Syphilis/HIV Point-of-Care Diagnostic Test (MBIO)

PATH

Status

Completed

Conditions

Syphilis

HIV

Treatments

Device: MBIO POC combined HIV syphilis test ( SnapEsi)

Study type

Interventional

Funder types

Other

Other U.S. Federal agency

Identifiers

NCT01530672

HS647

Details and patient eligibility

About

This is a diagnostic validation study for a combined Syphilis/HIV test made by MBio Diagnostics, Inc (MBio, Boulder, CO, USA). Although the MBio Syphilis/HIV diagnostic platform is designed for use at point of care (POC), it is made to provide similar performance as reference standards. Diagnosing HIV and syphilis accurately with a single POC test will save time for clinic health workers and technicians, reduce loss-to follow-up caused by lengthy delays for lab-based tests, and save costs by eliminating the need for multiple tests. For this study, the sensitivity and specificity of the MBio HIV/Syphilis Serology System point-of-care diagnostic test will be determined using reference tests performed under controlled laboratory conditions. For this, clients receiving routine care in the ANCs at the New Nyanza Provincial General Hospital (NNPGH) and Kisumu District Hospital (KDH) will be consented to provide blood for the proposed study. Study volunteers will receive HIV and syphilis rapid tests provided as part of routine care, and will donate an additional blood for evaluating the MBio test against the reference tests in a laboratory setting. This study is an investigational prototype, not for product registration. The results from this study will be used to inform product development of a second iteration of the MBio device design. At the time that the device is ready to be registered, it will undergo another field evaluation at which time it will be submitted to the appropriate regulatory body. Because the MBIO device is an HIV test, the device would be submitted to National AIDS & STI Control Program (NASCOP), which is the appropriate regulatory body for HIV tests in Kenya.

Enrollment

2,900 patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Pregnant
Attending her first routine ANC visit and willing to undergo tests for HIV/syphilis
Able and willing to legally consent for enrollment
Able to demonstrate-comprehension of study details as they are explained in the consent process by passing all the test questions of understanding. The subject is only allowed two attempts at passing the test of understanding.

Exclusion criteria

Unwilling to provide written informed consent.
Unable to legally consent (minor without guardian)
Opt out of HIV or syphilis test
Previously diagnosed with autoimmune disorder (lupus, Lyme disease), as determined by client recollection or clinical record.