Scandinavian Candesartan Acute Stroke Trial (SCAST)

Phase 3

Completed

• Conditions: Stroke
• Interventions: Drug: Candesartan Cilexetil; Drug: Placebo

• Registration Number: NCT00120003
• Lead Sponsor: Ullevaal University Hospital

Brief Summary

The purpose of this trial is to assess whether the blood pressure lowering agent candesartan (an angiotensin receptor type 1 blocker) is effective when given to patients with acute stroke and elevated blood pressure.

Hypothesis:

AT1 receptor blockade with candesartan in acute stroke will:

1. reduce the risk of death or major disability at 6 months by a 6% absolute risk reduction, relative to placebo.

2. reduce the risk of the combined event of "vascular" death, myocardial infarction, or stroke during the first 6 months by a 25% relative risk reduction, relative to placebo

Detailed Description

It has long been a controversy whether elevated blood pressure should be lowered in the acute phase of stroke. Current clinical practice is generally to accept high blood pressure in the acute phase of stroke, to avoid reduction of cerebral blood perfusion. This practice has a well-founded theoretical basis, but is not supported by evidence from clinical trials. The newly published study ACCESS (Stroke 2003;34:1699) showed a clear beneficial effect of the angiotensin receptor blocker candesartan in the acute phase of stroke, but the trial was seriously underpowered.

The Scandinavian Candesartan Acute Stroke Trial (SCAST) is designed to provide reliable data on the effects of candesartan in a wide variety of patients with acute stroke (target recruitment 2,500). Patients presenting with acute stroke (\<30 hours) and systolic blood pressure ≥140 mm Hg will be randomly assigned to candesartan 4 to 16 mg once daily or matching placebo for 7 days, followed by candesartan treatment for 6 months for patients who are hypertensive at the end of the treatment period (at clinician's discretion). Follow-up will be performed double-blind at 30 days, 3 months and 6 months.

The trial is co-ordinated from Ullevaal University Hospital in Oslo, Norway. Over 100 centres from Norway, Sweden, Denmark and Belgium have agreed to participate. Financial contributors: The Eastern Norway Regional Health Authority, AstraZeneca, and Ullevaal University Hospital (Oslo). AstraZeneca will supply drugs and placebo for the trial.

Study Timeline

• Study Start: 2005-06
• Study First Submitted: 2005-07-06
• Study First Submitted QC: 2005-07-06
• Study First Posted: 2005-07-14
• Status Verified: 2006-09
• Primary Completion: 2010-09
• Study Completion: 2010-09
• Last Update Submitted: 2011-06-30
• Last Update Posted: 2011-07-01

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 2500

Inclusion Criteria

• Clinical stroke syndrome with limb paresis, not likely to represent a transient ischaemic attack or non-stroke pathology (e.g. cerebral tumour)
• Systolic blood pressure ≥ 140 mm Hg
• Trial treatment possible within 30 hrs of symptom onset. If time of onset is not known, use the time when the patient was last known to be well.
• Consent (subsidiary, assent from legal acceptable representative, or waiver of consent)
• Age >18 years

Exclusion Criteria

• Markedly reduced consciousness (i.e. Scandinavian Stroke Scale consciousness score ≤ 2)

• Patient already receiving AT1 receptor blocker

• Contraindication to treatment with AT1 receptor blocker, e.g.:

  • known renal failure (women: creatinine ≥ 150 µmol/L; men: ≥ 180 µmol/L)
  • previously diagnosed bilateral renal artery stenosis
  • previously diagnosed high-grade aortic stenosis
  • previously diagnosed seriously impaired liver function and/or cholestasis
  • known intolerance to candesartan or other tablet ingredients

• Clear indication, in the clinician's view, for start of treatment with AT1 receptor blocker during the treatment period (e.g. chronic heart failure grade III-IV, in the presence of intolerance to ACE inhibitors)

• Clear indication, in the clinician's view, for antihypertensive therapy during the acute phase of stroke (i.e. concurrent hypertensive encephalopathy or aortic dissection, or other situations)

• Other serious or life-threatening disease before the stroke:

• Patient severely mentally or physically disabled (e.g. Mini Mental Status score < 20, or modified Rankin Scale score ≥ 4)

• Life expectancy < 12 months

• Patient unavailable for follow-up (e.g. no fixed address)

• Pregnant or breast-feeding woman

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Candesartan Cilexetil	Candesartan Cilexetil	Candesartan Cilexetil
Placebo	Placebo	Placebo

Primary Outcome Measures

Name	Time	Method
Death or major disability (defined by the modified Rankin scale) at 6 months	6 months
The composite event "vascular" death, myocardial infarction, or stroke during the first 6 months	6 months

Secondary Outcome Measures

Name	Time	Method
EuroQol score at 6 months	6 months
Myocardial infarction	6 months
Renal failure	7 days
Mini-Mental State score at 6 months	6 months
Death (all-cause death and "vascular" death)	6 months
Recurrent stroke (ischaemic, haemorrhagic, or unspecified)	6 months
Scandinavian Stroke Scale score at 7 days	7 days
Barthel Index score at 6 months	6 months
Combination of the above events	6 months
Symptomatic hypotension	7 days

Trial Locations

Locations (1)

Ullevaal University Hospital; 🇳🇴 Oslo, Norway