Evaluation of a Diagnostic Device, CL Detect™ Rapid Test, for the Diagnosis of Cutaneous Leishmaniasis in Peru

UnknownOBSERVATIONAL

Enrollment

200

Participants

Timeline

Start Date

October 2, 2018

Primary Completion Date

March 31, 2019

Study Completion Date

April 30, 2019

Conditions

Leishmaniasis, Cutaneous

Interventions

DEVICE

CL Detect™ Rapid Test

Observational study of a FDA cleared device, the CL Detect™ Rapid Test.

Trial Locations (2)

RECRUITING

Universidad Peruana Cayetano Heredia (UPCH), Lima

RECRUITING

U.S. Naval Medical Research Center Unit No. 6 (NAMRU-6), Puerto Maldonado