Recruitment

Recruitment Status
Completed

Summary

Conditions
Cutaneous Leishmaniases
Type
Observational
Design
Observational Model: Case-ControlTime Perspective: Prospective

Participation Requirements

Age
Between 2 years and 125 years
Gender
Both males and females

Description

The investigators enrolled 274 CL suspects in the study to determine the diagnostic performance of LoopampTM Leishmania Detection Kit and CL DetectTM Rapid Test for CL diagnosis in Afghanistan. The study was conducted at the National Malaria & Leishmaniasis Control Program (NMLCP) Leishmaniasis Clin...

The investigators enrolled 274 CL suspects in the study to determine the diagnostic performance of LoopampTM Leishmania Detection Kit and CL DetectTM Rapid Test for CL diagnosis in Afghanistan. The study was conducted at the National Malaria & Leishmaniasis Control Program (NMLCP) Leishmaniasis Clinic in Kabul, Afghanistan.

Tracking Information

NCT #
NCT03435419
Collaborators
Not Provided
Investigators
Principal Investigator: Martijn Vink, MD, MPH HealthNet TPO Study Director: Israel Cruz, PhD Foundation for Innovative New Diagnostics