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Completed Phase 3 Interventional Results available

[SOCRATES -Acute Stroke Or Transient IsChaemic Attack TReated With Aspirin or Ticagrelor and Patient OutcomES]

ClinicalTrials.gov ID: NCT01994720

Public ClinicalTrials.gov record NCT01994720. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 1:55 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomised, Double-Blind, Multinational Study to Prevent Major Vascular Events With Ticagrelor Compared to Aspirin (ASA) in Patients With Acute Ischaemic Stroke or TIA.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objective of the study is to compare the effect of 90-day treatment with ticagrelor (180 mg \[two 90 mg tablets\] loading dose on Day 1 followed by 90 mg twice daily maintenance dose for the remainder of the study) vs acetylsalicylic acid (ASA)-aspirin (300 mg \[three 100 mg tablets\] loading dose on Day 1 followed by 100 mg once daily maintenance dose for the remainder of the study) for the prevention of major vascular events (composite of stroke, myocardial infarction \[MI\], and death) in patients with acute ischaemic stroke or transient ischaemic attack (TIA).

Study identification

NCT ID
NCT01994720
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
13,307 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years to 130 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 7, 2014 (Actual)
Primary completion
Mar 2, 2016 (Actual)
Completion
Mar 2, 2016 (Actual)
Last update posted
Jun 12, 2017

2014 – 2016

United States locations

U.S. sites
115
U.S. states
35
U.S. cities
115
Facility City State ZIP Site status
Research Site Montgomery Alabama — —
Research Site Phoenix Arizona — —
Research Site Fayetteville Arkansas — —
Research Site Fort Smith Arkansas — —
Research Site Fullerton California — —
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Research Site Frederick Maryland — —
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Research Site Pontiac Michigan — —
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Research Site Robbinsdale Minnesota — —
Research Site Saint Paul Minnesota — —
Research Site Bridgeton Missouri — —
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Research Site Albuquerque New Mexico — —
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Research Site Roanoke Virginia — —
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Research Site Huntington West Virginia — —
Research Site Morgantown West Virginia — —
Research Site Milwaukee Wisconsin — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 406 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01994720, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 12, 2017 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01994720 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →