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OpenTrials
Completed

NCT Number: NCT00147602

Lipitor In The Prevention Of Stroke, For Patients Who Have Had A Previous Stroke

To determine whether Lipitor reduces stroke, compared to placebo in patients who have had a previous stroke or transient ischemic attack.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Pfizer Investigational Site, East Gosford, New South Wales, Australia

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Previous stroke or TIA

Exclusion criteria

  • coronary heart disease

Treatment and study plan

atorvastatin

Drug

Primary outcomes

  1. Time to occurrence of fatal or non-fatal stroke

Secondary outcomes

  1. Time to occurrence of an acute coronary event, consisting of cardiac death, nonfatal myocardial infarction, resuscitated cardiac arrest or unstable angina.

  2. Time to occurrence of a cerebrovascular event, defined as fatal or nonfatal stroke or TIA.

Sponsors and collaborators

Lead sponsor

Pfizer

Industry

Registry information

Official study title

A Double-Blind, Randomized, Placebo- Controlled Study Of Atorvastatin As Prevention Of Cerebrovascular Events In Patients With A Previous Transient Ischemic Attack (TIA) Or Stroke

Acronym: SPARCL

Important dates

Study start
1998
Study completion
2005
First posted
Sep 7, 2005
Registry last updated
Apr 22, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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