Either you have JavaScript disabled or your browser does not support Javascript . To work properly, this page requires JavaScript to be enabled.
How to enable JavaScript in your browser?

Prospective randomized phase IV open label comparative study of dalteparin [fragmin] vs unfractionated heparin for the prevention of venous thromboembolism (VTE) in hospitalized acutely ill medical patients.

Next Previous
X
Search
Trial Profile

Prospective randomized phase IV open label comparative study of dalteparin [fragmin] vs unfractionated heparin for the prevention of venous thromboembolism (VTE) in hospitalized acutely ill medical patients.

Status: Discontinued
Phase of Trial: Phase IV

Latest Information Update: 08 Oct 2009

Price : $35 *
  • Adis is an information provider.
  • Final gross price and currency may vary according to local VAT and billing address.
  • Your purchase entitles you to full access to the information contained in our trial profile at the time of purchase.
  • A link to download a PDF version of the trial profile will be included in your email receipt.

At a glance

  • Drugs Dalteparin sodium (Primary) ; Heparin
  • Indications Deep vein thrombosis; Pulmonary embolism; Thromboembolism
  • Focus Therapeutic Use
  • Sponsors Pfizer

    • Most Recent Events

    • 16 Dec 2008 Planned number of patients changed from 360 to 84.
    • 25 Sep 2008 Study start date changed from Aug 2007 to Jul 2007 as reported by CT.gov
    • 25 Sep 2008 Status changed from recruiting to discontinued as reported by CT.gov

You need to be a logged in or subscribed to view this content Request demo

If your organization or you do not have a subscription, try one of the following:
  • Contacting your organization’s admin about adding this content to your AdisInsight subscription
  • Buying a PDF version of any individual profile
  • Request a free trial
If your organization has a subscription, there are several access options, even while working remotely:
  • Working within your organization’s network
  • with username/password or try to via your institution
  • Persisted access using your organization’s identifier stored in your user browser for 90 days
Back to top