HIV
Conditions
Interventions
None listed
Sponsors
Keio University School of Medicine Centor for Infectious Disease and Infection Control
Negishi Clinic
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: HIV-positive patients 20 years or older Written informed consent obtained from the subject.
Exclusion criteria
Exclusion criteria: Patients during pregnancy or lactation Patients who we consider inappropriate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. HIV tropism 2. relationship between HIV tropism and patient backgrounds A Patient backgrounds(age,sex,date of diagnosis, HIV-RNA, CD4 counts at diagnosis, lowest CD4 counts, treatment history, regimen/dose/treatment term, drugs, AIDS history) B drug concentrations in blood C drug concentrations in hair and saliva D HIV-RNA in saliva E drug susceptibility F HIV-RNA and CD4 counts at the time of HIV tropism testing G metabolic marker such as bone density at the time of HIV tropism testing | — |
Secondary
| Measure | Time frame |
|---|---|
| Time course of above factors | — |
Countries
Japan
Contacts
Public ContactNaoki Hasegawa
Keio University School of Medicine Centor for Infectious Disease and Infection Control
Outcome results
None listed