Immune Effects of Vitamin D in Hemodialysis Patients

PHASE2CompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

December 31, 2004

Primary Completion Date

September 30, 2007

Study Completion Date

September 30, 2007

Conditions
End Stage Renal DiseaseHemodialysisInflammatory ResponseCardiovascular Disease
Interventions
DRUG

paricalcitol

Dosage Form: Intravenous administration. Dosage: 0.01 micrograms/kilogram of body weight. Frequency: 2 HD treatments of each study week (depending on phase of study). Duration: 4 weeks.

Trial Locations (3)

10003

Irving Place Dialysis Center, New York

10025

Upper Manhattan Dialysis Center, New York

10128

Yorkville Dialysis Center, New York

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Abbott

INDUSTRY

lead

Renal Research Institute

OTHER

NCT00686751 - Immune Effects of Vitamin D in Hemodialysis Patients | Biotech Hunter | Biotech Hunter