| Trial ID: | L1282 |
| Source ID: | NCT00298441
|
| Associated Drug: |
Chondroitin Sulfate-Iron Colloid
|
| Title: |
Efficacy of Intravenous Iron Administration in Hemodialysis Patients
|
| Acronym: |
|
| Status: |
COMPLETED
|
| Study Results: |
NO
|
| Results: |
|
| Conditions: |
Chronic Renal Failure|Hemodialysis|Renal Anemia|Iron Deficiency Anemia
|
| Interventions: |
DRUG: chondroitin sulfate-iron colloid
|
| Outcome Measures: |
Primary: hemoglobin levels at 24 weeks|oxidized albumin levels at 24 weeks |
|
| Sponsor/Collaborators: |
Sponsor: Kumamoto University
|
| Gender: |
ALL
|
| Age: |
ADULT, OLDER_ADULT
|
| Phases: |
PHASE4
|
| Enrollment: |
50
|
| Study Type: |
INTERVENTIONAL
|
| Study Designs: |
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: TREATMENT
|
| Start Date: |
2005-06
|
| Completion Date: |
2007-03
|
| Results First Posted: |
|
| Last Update Posted: |
2008-05-12
|
| Locations: |
Midorigaoka Clinic, Arao, Kumamoto, 864-0033, Japan|Kumamoto University Hospital, Kumamoto, 860-8556, Japan
|
| URL: |
https://clinicaltrials.gov/show/NCT00298441
|
