Cyanocobalamin Injection |
Crystamine; Crysti 1000; Cyanoject; Cyomin; Rubesol-1000; Vitamin B-12 Injection |
Clinical Trial: Randomized Study of Folic Acid Therapy for Hyperhomocysteinemia in Patients with End Stage Renal Disease Receiving Hemodialysis
This study is currently recruiting patients.
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Purpose
OBJECTIVES: I. Compare the efficacy of two doses of folic acid in normalizing plasma total homocysteine concentration in patients with end stage renal disease receiving regular hemodialysis therapy resulting in hyperhomocysteinemia. II. Determine the requirement of co-supplementation with extra pyridoxine (vitamin B6) and cyanocobalamin (vitamin B12) daily in these patients. III. Assess the safety and tolerability of this therapy in these patients.
| Condition | Treatment or Intervention |
|---|---|
| End Stage Renal Disease Hyperhomocysteinemia | Drug: cyanocobalamin Drug: folic acid Drug: pyridoxine |
MedlinePlus related topics: Genetic Disorders; Kidney Failure; Metabolic Disorders
Study Type: Interventional
Study Design: Treatment, Efficacy Study
Expected Total Enrollment: 84
Study start: June 1999
PROTOCOL OUTLINE: This is a randomized, placebo controlled study. Patients are stratified according to prestudy homocysteine levels (above or below average). Patients are randomized to receive placebo or one of two doses of oral folic acid, with or without pyridoxine and cyanocobalamin. Arm I: Patients receive oral placebo daily. Arm II: Patients receive oral pyridoxine, cyanocobalamin, and oral placebo daily. Arm III: Patients receive oral pyridoxine, cyanocobalamin, and folic acid daily. Arm IV: Patients receive oral pyridoxine and cyanocobalamin plus a higher dose of folic acid daily. Arm V: Patients receive oral placebo and oral folic acid daily. Arm VI: Patients receive oral placebo and higher dose folic acid daily. Treatment continues for 8 weeks.
Eligibility
Ages Eligible for Study: 21 Years - 89 Years, Genders Eligible for Study: Both
Criteria
PROTOCOL ENTRY CRITERIA:
--Disease Characteristics--
- Diagnosis of end stage renal disease requiring regular hemodialysis treatment 3 times weekly
- Baseline predialysis total homocysteine concentration in plasma greater than 16 micromoles/L
- No prior or concurrent pernicious anemia
- No blood smear examination showing unexplained macrocytosis
--Prior/Concurrent Therapy--
- Chemotherapy: No concurrent chemotherapy for cancer
- Other: No concurrent levodopa or carbidopa No concurrent penicillamine or trimethoprim-sulfonamide combination No concurrent antiviral therapy No concurrent anticonvulsants
--Patient Characteristics--
- Hematopoietic: Hematocrit at least 25%
- Other: Not pregnant or nursing Negative pregnancy test Fertile patients must use effective contraception No Parkinson's disease No convulsions or epilepsy requiring treatment No lactose intolerance or allergy to milk products No history of allergic sensitization following administration of folic acid, pyridoxine (vitamin B6), or cyanocobalamin (vitamin B12) No vitamin B12 concentration below lower limit of normal (150 picamole/L) No untreated hypothyroidism or psoriasis
Location and Contact Information
District of Columbia
Georgetown University Medical Center, Washington, District of Columbia, 20007, United States; Recruiting
Christopher S. Wilcox, Study Chair, Georgetown University
More Information
Record last reviewed: August 1999
Last Updated: October 22, 2004
Record first received: October 18, 1999
ClinicalTrials.gov Identifier: NCT00004495
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005
Resources
- Crystamine (Drug Digest)
- Crysti 1000 (Drug Digest)

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