HOPE in Action Trial of HIV+ Deceased Donor Liver Transplants for HIV+ Recipients
NCT03734393
Acquired Immunodeficiency Syndrome, Blood-Borne Infections
Birmingham, Alabama, United States
View Trial DetailsNCT Number: NCT00339612
This is an observational, prospective cohort study to describe the demographic, clinical, immunologic, and virologic characteristics of HIV-infected children at participating clinical sites in Latin American countries. Enrollment in this study will consist of approximately 500 HIV-infected children in two cohorts who acquired HIV infection through mother-to-child transmission (MTCT). The first group will be a static cohort consisting of HIV-infected children who were five years of age or younger when previously enrolled into the NISDI Pediatric Protocol. The second cohort will be a dynamic cohort of prospectively enrolled, HIV-infected children who are five years of age or younger. We will characterize complications from both the disease and its treatments. Subjects will be evaluated every six months for approximately five years and assessments of growth, morbidity, disease progression and mortality will be made.
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Notify MeUp to 21 year
All sexes
Observational
Universidade Federal de Minas Gerais, Belo Horizonte, Brazil
This is an observational, prospective cohort study to describe the demographic, clinical, immunologic, and virologic characteristics of HIV-infected children at participating clinical sites in Latin American countries. Enrollment in this study will consist of approximately 500 HIV-infected children in two cohorts who acquired HIV infection through mother-to-child transmission (MTCT). The first group will be a static cohort consisting of HIV-infected children who were five years of age or younger when previously enrolled into the NISDI Pediatric Protocol. The second cohort will be a dynamic cohort of prospectively enrolled, HIV-infected children who are five years of age or younger. We will characterize complications from both the disease and its treatments. Subjects will be evaluated every six months for approximately five years and assessments of growth, morbidity, disease progression and mortality will be made.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Static Cohort:
Dynamic cohort:
Exclusion criteria
Time frame: q 6 months
characterize complications from both the disease and its treatments
Time frame: q 6 months
characterize complications from both the disease and its treatments
Time frame: q 6 months
characterize complications from both the disease and its treatments
Time frame: q 6 months
characterize complications from both the disease and its treatments
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Nih
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