LV Thrombus Pilot Study for Comparing Enoxaparin Vs. Warfarin

NCT00321009 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2006-05-03

No results posted yet for this study

Summary

To prospectively evaluate the utility of enoxaparin vs. oral warfarin in reduction of echocardiographic indices of LV mural thrombus. The primary outcome is the presence of LV mural thrombus at 3.5 months. The secondary outcome is cost analysis comparing the two arms.

Conditions

Interventions

DRUG

Enoxaparin

Sponsors & Collaborators

  • Rhone-Poulenc Rorer

    collaborator INDUSTRY
  • William Beaumont Hospitals

    lead OTHER

Principal Investigators

  • Cindy L Grines, MD · William Beaumont Hospitals

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2000-03-31
Completion
2004-04-30

Countries

  • United States

Study Locations

More Related Trials

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 NCT00321009 on ClinicalTrials.gov