Clinical trial
To Determine the Feasibility of a Clinical Trial Comparing Anticoagulants Versus…
NCT00238667 · St George's, University of London, Other · Completed
Key facts
| NCT number | NCT00238667 |
|---|---|
| Title | To Determine the Feasibility of a Clinical Trial Comparing Anticoagulants Versus Antiplatelets in the Acute Treatment of Patients With Cervical Artery Dissection |
| Official title | Cervical Artery Dissection in Stroke Study |
| Acronym | CADISS |
| Lead sponsor | St George's, University of London, Other |
| Collaborators | The Stroke Association, United Kingdom |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Cervical Artery Dissection, Carotid Artery Dissection, Vertebral Artery Dissection, Stroke |
| Intervention type | Drug |
| Interventions | Antiplatelet (Aspirin, Dipyridamole, clopidogrel), Anticoagulant (Unfractionated Heparin, LMW Heparin, Warfarin) |
| Enrollment | 250 |
| Start date | Nov 1, 2005 |
| Completion | May 1, 2014 |
| First posted | Oct 13, 2005 |
| Last update posted | May 20, 2015 |
| Countries | United Kingdom |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: