- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00401349
Expression of Mif Alleles in Individuals With Leishmaniasis
March 27, 2020 updated by: Yale University
Immune and Inflammatory Responses in L. (Viannia) Infection Aim 2: Expression of Mif Alleles in Individuals With Recurrent Leishmaniasis, Chronic Leishmaniasis and Asymptomatic Infection
CIDEIM, Centro Internacional de Entrenamiento e Investigaciones Medicas, is conducting a research study about the disease Cutaneous Leishmaniasis, which is caused by the Leishmania parasite and causes skin sores.
Researchers hope to find out how the human body defends against Leishmania.
A total of 472 individuals, ages 7 to 70 years, belonging to one of the following groups will be included in this study: recurring disease, chronic disease, disease with no sign or symptoms (asymptomatic), and healthy individuals.
Study procedures will include a questionnaire and buccal swab (swabbing of the inside of the cheek with a cotton or wooden applicator).
In addition, asymptomatic and healthy individuals will provide a blood sample.
Study participation will be up to 1.5 hours.
Study Overview
Status
Completed
Conditions
Detailed Description
The purpose of this study is to define the proportion of low and high expression Mif alleles in individuals with recurrent or chronic Cutaneous Leishmaniasis and compare it with that of individuals with asymptomatic infection and healthy donors (controls), in order to determine if these alleles are associated with outcome of infection.
This study is part 2 of a project that includes DMID protocols 05-0139 and 06-0010.
Specific objectives are to: determine the proportion of low expression (5-CATT) Mif alleles in individuals with recurrent or chronic cutaneous leishmaniasis, healthy donors (controls), and individuals with asymptomatic infection; determine the proportion of high expression (6,7,8-CATT) Mif alleles in individuals with recurrent or chronic cutaneous leishmaniasis, healthy donors (controls), and individuals with asymptomatic infection; and determine the Mif Genotype repertoire and frequency distribution in the endemic population of study.
This study will be conducted in 472 participants who will be enrolled into one of the following 4 groups: recurrent disease, chronic disease, asymptomatic infection, and healthy donors (controls).
Patients (males and females) aged between 7-70 years with chronic or recurrent cutaneous leishmaniasis (historic or active) diagnosed in either Cali (CIDEIM) and Tumaco (San Andrés Hospital) on the Colombian Pacific Coast will be invited to participate in the study.
Asymptomatic and healthy donors (controls) will also be enrolled.
Pregnant women will not be enrolled.
Consent and samples will be obtained during a single study visit of up to 1.5 hours.
No further follow-up visits are planned for this study.
Genetic material extracted and amplified from buccal swabs will be used to determine the proportion of low and high expression Mif alleles of each group.
Expression in recurrent and chronic participants will be compared to that of asymptomatic participants and healthy donors (controls) in order to determine if expression frequencies are related to the outcome of infection.
Blood samples obtained from asymptomatic and healthy donors will undergo in vitro blastogenesis testing to confirm asymptomatic/healthy donor status.
Study outcome measures are: frequency of low expression (5-CATT) Mif alleles in participants with recurrent or chronic disease, individuals with asymptomatic infection and healthy donors (controls); frequency of high expression (6,7,8-CATT) Mif alleles in participants with recurrent or chronic disease individuals with asymptomatic infection and healthy donors (controls); and Mif Genotype repertoire and frequency distribution in the endemic population in the study site.
Study Type
Observational
Enrollment (Actual)
438
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Cali, Colombia
- Centro Internacional de Entrenamiento e Investigaciones Medicas, CIDEIM
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
7 years to 70 years (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
- Active or historical cases of recurrent cutaneous leishmaniasis
- Active or historical cases of chronic or recurrent cutaneous leishmaniasis
- Endemic area controls - Resident of endemic area with no history or evidence of active or prior dermal leishmaniasis
- Healthy donors (non-exposed to leishmaniasis)
Description
Inclusion Criteria:
Active or historical cases of recurrent cutaneous leishmaniasis
- Age 7-70 years
- History of parasitologically confirmed (at time of diagnosis) recurrent leishmaniasis
- Voluntary participation in the study
- Written and signed Informed consent/assent forms
Active or historical cases of chronic cutaneous leishmaniasis
- Age 7-70 years
- History of parasitologically confirmed (at time of diagnosis) chronic leishmaniasis
- Voluntary participation in the study
- Written and signed Informed consent/assent forms
Asymptomatic infection
- Age 7-70 years
- Resident of endemic area
- No history or evidence of active or prior dermal leishmaniasis
- Voluntary participation in the study
- Written and signed Informed consent/assent forms
Healthy donors
- Age 7-70 years
- No history or evidence of exposure to transmission of leishmaniasis
- Voluntary participation in the study
- Written and signed Informed consent/assent forms
Exclusion Criteria:
Pregnancy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Prospective
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
December 1, 2006
Study Completion (Actual)
April 1, 2010
Study Registration Dates
First Submitted
November 16, 2006
First Submitted That Met QC Criteria
November 16, 2006
First Posted (Estimate)
November 20, 2006
Study Record Updates
Last Update Posted (Actual)
March 30, 2020
Last Update Submitted That Met QC Criteria
March 27, 2020
Last Verified
August 1, 2011
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0608001742
- U19AI065866 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.