Pharmacokinetic Study of Fondaparinux in Outpatients With Renal Dysfunction

NCT00483600 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2014-07-29

No results posted yet for this study

Summary

To determine the appropriate dose and safety of a preventative dose of fondaparinux, an anticoagulant medication (blood thinner) in patients with kidney disease.

Conditions

Interventions

DRUG

fondaparinux

injections of 2.5mg every other day for 4 weeks

Sponsors & Collaborators

Principal Investigators

  • Thomas L Ortel, PhD · Duke University

Study Design

Allocation
NON_RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-08-31
Completion
2008-08-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00483600 on ClinicalTrials.gov