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Clinical Trials/NCT00001169
NCT00001169
Completed
Not Applicable

Clinical Investigation of Infections Due to Leishmanial Parasites

National Institute of Allergy and Infectious Diseases (NIAID)1 site in 1 country250 target enrollmentDecember 10, 2002

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Leishmaniasis
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Enrollment
250
Locations
1
Status
Completed
Last Updated
18 years ago

Overview

Brief Summary

Mechanisms of host immune response to intracellular protozoa will be investigated in patients with naturally acquired infection employing a variety of in-vitro techniques. Both non-specific and antigen-specific humoral and cellular immune responses will be assessed. Parasites will be isolated from patients, cultivated in-vitro, and characterized. Responses to chemotherapy will be assessed parasitologically, immunologically and clinically.

Detailed Description

The main purpose of this protocol is to permit us to see patients who are referred to us for diagnosis and treatment of known or suspected leishmaniasis (from the Peace Corps, Smithsonian Institution, tourists, etc.). In the process of working up these patients, we sometimes encounter parasite isolates that are useful for research. We also can perform tests of cell-mediated immune function to evaluate how patients are responding to therapy. In addition, the protocol permits us to observe therapeutic responses to other drugs besides pentavalent antimony, if necessary.

Registry
clinicaltrials.gov
Start Date
December 10, 2002
End Date
February 2001
Last Updated
18 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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