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NCT05300737: SCORE

Symptomatic Carotid Outcomes Registry With Multi-center Evaluation

Active, enrolled Last updated 15 October 2025
What this trial tests

trial testing intensive medical therapy in Carotid Stenosis in 114 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
1 August 2022
Primary endpoint
1 December 2026
1 December 2026

Quick facts

Lead sponsorUniversity of Maryland, Baltimore
StatusActive, enrolled
Study typeOBSERVATIONAL
Enrollment114
Start date1 August 2022
Primary completion1 December 2026
Estimated completion1 December 2026
Sites18 locations across United States, Canada

Drugs / interventions tested

Conditions studied

Sponsor

University of Maryland, Baltimore

Who can join

40 and older, any sex, with Carotid Stenosis or Ischemic Stroke. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The purpose of this study is to build upon trials done over 30 years ago, which did not include statins, new antiplatelet agents, and newer antihypertensive medications. Since the landmark trials (NASCET, ECST), there have been new developments in medical stroke prevention, which creates a gap in knowledge. The aim of this study is to evaluate that clinical care with Intensive Medical Therapy (IMT) alone, the one year stroke rate in patients with symptomatic carotid stenosis and low risk clinical features will be \<5%.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Carotid Stenosis

Currently open trials in the same condition.

Other University of Maryland, Baltimore trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05300737.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing