Yaws Clinical Trial
Official title:
Evaluation of a Rapid Dual Point-of-care Assay for Targeting Antibiotic Treatment for Yaws Eradication: a Prospective Descriptive Study
A dual POC immunoassay simultaneously detecting non-treponemal and treponemal antibodies was developed for the diagnosis of infections with T. pallidum. The assay is designed for use in resource-limited settings where challenging conditions (such as lack of electricity, running water, or laboratory equipment) commonly exist. We sought to compare performance of the dual-POC assay for diagnosis of yaws infection with that of the RPR and TPHA as reference standards.
Yaws is an infectious disease caused by Treponema pallidum subspecies pertenue, a bacterium
which closely resembles the causative agent of syphilis, and is spread by skin to skin
contact. In the field, yaws is diagnosed on the basis of epidemiological context, evocative
symptoms and signs and positive serological tests or dark field microscopy. The darkfield
microscopy is not easy to perform , hence the interest in serological tests. The serological
tests used to confirm yaws are the same as those used to diagnose syphilis. Yaws serologic
diagnosis relies on testing for non-treponemal and treponemal antibodies. These antibodies
differ markedly with respect to antigenic reactivities and kinetics during the disease
process.
Historically screening for yaws has involved the use of nontreponemal tests, such as rapid
plasma reagin or venereal disease research laboratory. Positive results of nontreponemal
tests of specimens are then confirmed using a more specific treponemal test, such as
Treponema pallidum haemagglutination. However, the equipment and personnel requirements for
conducting and interpreting these laboratory-tests are rarely available in low-resource
settings in developing countries where yaws occurs.
Rapid treponemal tests which detect antibodies to T. pallidum antigen have become popular
for the diagnosis of venereal syphilis due to their many advantages. These tests that can be
performed outside a laboratory setting with minimal training and using blood collected by a
finger prick, which makes them extremely useful in remote areas where laboratories are not
available. However, the rapid treponemal tests for syphilis detect treponemal antibodies,
which limits their use for interpretation of the disease status since they cannot
distinguish between active and past or treated infection.
A combined point-of-care (POC) test which detects both treponemal and non-treponemal
antibodies has recently been evaluated for the diagnosis of syphilis, and appears promising
for yaws diagnosis. The use of the dual POC test would result in the ability to both screen
and confirm the serological status of patients with suspected yaws within 15 minutes and
give a better indication of active disease.
;
Observational Model: Cohort, Time Perspective: Prospective
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT01382004 -
Single-dose Azithromycin for the Treatment of Yaws
|
Phase 3 | |
Completed |
NCT03664063 -
PK PD Study of IDA and Azithromycin for NTDs ( ComboNTDs )
|
Phase 2 | |
Completed |
NCT03676140 -
Safety of Co-administration of IDA and Azithromycin for NTDs ( ComboNTDs )
|
Phase 3 | |
Completed |
NCT04453124 -
An Accessible Low-cost Plant Treatment for Cutaneous Ulcers
|
Phase 2 | |
Completed |
NCT01955252 -
Effect of WHO-yaws Elimination Strategy in Lihir Island, Papua New Guinea
|
Phase 3 | |
Active, not recruiting |
NCT04753788 -
Evaluation of a LAMP Assay for T. Pallidum. Pertenue
|
||
Active, not recruiting |
NCT05764876 -
Repurposing Clinically Approved Drugs for Yaws With an Insight Into the Cutaneous Ulcer Disease Syndrome (Trep-AByaws)
|
Phase 3 | |
Completed |
NCT02344628 -
Comparison of Two Different Doses of Azithromycin for Treatment of Yaws
|
Phase 3 | |
Completed |
NCT03683745 -
Integrated Mapping of Skin-presenting Neglected Tropical Diseases in Liberia
|
||
Completed |
NCT02775617 -
Azithromycin - Ivermectin Mass Drug Administration for Skin Disease
|
Phase 4 | |
Completed |
NCT03490123 -
Evaluation of an Intensive 3-round MDA Strategy Towards Yaws Eradication
|
Phase 4 |