At a glance
ClinicalIndex Comparison RecordN/ACompleted· 168 enrolled
Drug / intervention
No Interventionother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Evaluation of a Diagnostic Device, CL Detect Rapid Test, for the Diagnosis of Cutaneous Leishmaniasis in Tunisia
U.S. Army Medical Research and Development Command·observational·Posted Jan 16, 2013·Updated Jun 20, 2017
In Brief
An observational study evaluating No Intervention for Skin Diseases, Parasitic. Completed, enrolled 168 participants across 2 sites.
Detailed Summary
The purpose of the study is to evaluate the sensitivity and specificity of CL Detect, in subjects with suspected CL in Tunisia.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsSkin Diseases, Parasitic
CountriesTunisia
CollaboratorsInBios International, Inc., Institut Pasteur of Tunis, Tunisia
Timeline
N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
Enrollment StartJan 2013
First PostedJan 2013
Primary CompletionAug 2013
Study CompletionApr 2014
TodayJul 2026
First PostedJan 16, 2013
Enrollment StartJan 1, 2013
Primary CompletionAug 1, 2013
Study CompletionApr 1, 2014
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 13.5 years ago
Interventions
No Interventionother