Fanconi Syndrome Due to ARVs in HIV-Infected Persons

NCT00499187 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 56

Last updated 2014-03-17

No results posted yet for this study

Summary

Cross-sectional cohort study of participants with HIV with or without protocol-defined Fanconi syndrome (confirmed creatinine clearance \[CLcr\] decline and evidence of proximal tubulopathy).

Conditions

Interventions

PROCEDURE

Blood Draws

A single whole blood sample was collected for genomic analysis.

Sponsors & Collaborators

Principal Investigators

  • John Flaherty, PharmD · Gilead Sciences

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-09-30
Primary Completion
2011-03-31
Completion
2011-03-31

Countries

  • United States
  • Canada

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00499187 on ClinicalTrials.gov