Overview

Acute Candesartan Cilexetil Outcomes Stroke Trial (ACCOST)

Status:
Unknown status
Trial end date:
2007-09-01
Target enrollment:
Participant gender:
Summary
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.
Phase:
Phase 4
Details
Lead Sponsor:
City Hospitals Sunderland NHS Foundation Trust
Collaborator:
Takeda
Treatments:
Candesartan
Candesartan cilexetil