Acute Candesartan Cilexetil Outcomes Stroke Trial (ACCOST)
Active, not recruiting
Phase 4 Results N/ASummary of Purpose
The aim of this study is to determine whether it is safe and effective to give the Angiotensin Receptor Blocker (ARB) Candesartan within the first 72 hours following acute stroke.
Read More →Trial Milestones
The following dates are available for this trial. Trial information last updated on 11 September 2006.
| 1 Dec 2004 | 18 Apr 2005 | Unavailable | 1 Sep 2007 | 1 Sep 2006 | Unavailable |
| Start Date | First Received | 1st Completion | Completion | Verification | Results |
|---|
Trial Basics
Interventions
Conditions
Sponsors
Trial Design
- Allocation: Randomized
- Masking: Double-Blind
- Purpose: Treatment
- Endpoint: Safety/Efficacy Study
- Intervention: Parallel Assignment
Contacts
Not available
View Trial Locations
Recruitment
- Enrollment: 50
- Gender: Both
- Minimum Age: 18 Years
- Accepts Healthy Volunteers: No
- 1 location, 1 country
Principal Investigator
- Christopher S Gray, MD
University of Newcastle Upon-Tyne
