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Clinical Trial Details

Trial ID: L0495
Source ID: NCT00338468
Associated Drug: Epoetin Alfa
Title: A Study to Assess Disability in Anemic Elderly Patients With Kidney Disease Receiving PROCRIT (Epoetin Alfa)
Acronym:
Status: TERMINATED
Study Results: NO
Results:
Conditions: Anemia|Kidney Diseases
Interventions: DRUG: epoetin alfa
Outcome Measures: Primary: Change in physical function score as measured by the Six Minute Walk Test (6MWT) and Short Physical Performance (SPP) Summary Score compared from Baseline to Week 5, Week 9, Week 13, Week 17/ Early Withdrawal and Week 20/Follow-up. | Secondary: Proportion of patients who achieve the target hemoglobin levels of > 13.0 g/dL and < =14.0 g/dL (independent of transfusion within 1 month of assessment) compared from Baseline to Week 5, Week 9, Week 13, Week 17/ Early Withdrawal and Week 20/Follow-up.
Sponsor/Collaborators: Sponsor: Ortho Biotech Products, L.P.
Gender: ALL
Age: OLDER_ADULT
Phases: PHASE4
Enrollment: 13
Study Type: INTERVENTIONAL
Study Designs: Allocation: NON_RANDOMIZED|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: TREATMENT
Start Date: 2003-11
Completion Date: 2005-09
Results First Posted:
Last Update Posted: 2011-05-19
Locations:
URL: https://clinicaltrials.gov/show/NCT00338468