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NCT00004495 · ClinicalTrials.gov registry record · NA

Randomized Study of Folic Acid Therapy for Hyperhomocysteinemia in Patients With End Stage Renal Disease Receiving Hemodialysis

A NA study, sponsored by Georgetown University.

Completed
Registry status
NA
Development phase
84
Enrollment target

NCT00004495 is a NA study that has completed, run by Georgetown University. The registered enrollment target is 84 participants.

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The verdict

NCT00004495, a NA study, has completed, sponsored by Georgetown University.

COMPLETED
Registry status
NA
Development phase
84 participants
Enrollment target

Study Summary

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.

Interventions

  • DRUG pyridoxine
  • DRUG cyanocobalamin
  • DRUG folic acid

Trial Details

FieldValue
Enrollment Target 84 participants
Start Date 1999-06
Est. Completion 2000-09
Phase NA

Sponsor

Georgetown University

227 total trials

What the Registry Record Tells You About NCT00004495

The ClinicalTrials.gov registry entry for NCT00004495 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 84 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Georgetown University, which has 227 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which pyridoxine is the first listed.

NCT00004495 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00004495 about?

NCT00004495 is a clinical study titled "Randomized Study of Folic Acid Therapy for Hyperhomocysteinemia in Patients With End Stage Renal Disease Receiving Hemodialysis". 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 pyr...

What is the current status of trial NCT00004495?

This trial is currently completed. It is a NA study. The enrollment target is 84 participants. The study started on 1999-06. Estimated completion is 2000-09.

What interventions are being tested in trial NCT00004495?

The interventions under investigation include: pyridoxine (DRUG), cyanocobalamin (DRUG), folic acid (DRUG).

Who is sponsoring clinical trial NCT00004495?

This trial is sponsored by Georgetown University, which has 227 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.