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Evaluation of a LAMP Assay for T. Pallidum. Pertenue (LAMP4YAWS)

L

London School of Hygiene and Tropical Medicine

Status

Completed

Conditions

Yaws

Treatments

Diagnostic Test: PCR
Diagnostic Test: LAMP

Study type

Observational

Funder types

Other

Identifiers

NCT04753788
LSHTM-21633

Details and patient eligibility

About

This is a diagnostic evaluation comparing the performance of real-time PCR performed at a national reference laboratory and a LAMP assay performed at a regional hospital for the diagnosis of yaws

Enrollment

563 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Lesion consistent with yaws
  • Positive treponemal and non-treponemal antibodies assessed by the DPP Syphilis Screen and Confirm RDT

Exclusion criteria

  • Unable to give consent

Trial design

563 participants in 1 patient group

Suspected Yaws Cases
Description:
Individuals with a lesion clinically suspected to be yaws and with evidence of positive treponemal and non-treponemal serology as assessed by point of care lateral flow tests (DPP Syphilis Screen and Confirm, Chembio)
Treatment:
Diagnostic Test: LAMP
Diagnostic Test: PCR

Trial documents
1

Trial contacts and locations

3

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Central trial contact

Rebecca Handley

Data sourced from clinicaltrials.gov

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