To Determine the Feasibility of a Clinical Trial Comparing Anticoagulants Versus Antiplatelets in the Acute Treatment of Patients With Cervical Artery Dissection "CADISS"

Completed

Phase 3 Results N/A

Summary of Purpose

This is a feasibility study to determine if a sufficient number of patients can be recruited throughout the United Kingdom and whether sufficient endpoints can be generated for a full scale therapeutic trial of anticoagulants versus antiplatelets in acute cervical artery dissection treatment.

Read More →

Trial Milestones

The following dates are available for this trial. Trial information last updated on 19 May 2015.

1 Nov 2005 11 Oct 2005 Unavailable 1 May 2014 1 Sep 2005 Unavailable
Start Date First Received 1st Completion Completion Verification Results

Trial Design

  • Allocation: Randomized
  • Masking: Open Label
  • Purpose: Treatment
  • Endpoint: Bio-equivalence Study
  • Intervention: Parallel Assignment
  • Observation: Defined Population
  • Perspective: Prospective

Contacts

Not available