Evaluating heart health in patients with acute ischemic stroke receiving reperfusion therapy

Heart Evaluation of Acute Ischemic Stroke With Reperfusion Therapy

Soochow University · NCT06882577

This study looks at how heart problems affect people who have had an acute ischemic stroke and are receiving treatment to see if it can help improve their care and outcomes.

Quick facts

Study typeObservational
Enrollment400 (estimated)
Ages18 Years and up
SexAll
SponsorSoochow University (other)
Locations1 site (Suzhou, Jiangsu)
Trial IDNCT06882577 on ClinicalTrials.gov

What this trial studies

This observational registry focuses on patients hospitalized for acute ischemic stroke who are undergoing reperfusion therapy. It aims to explore the relationship between heart diseases and acute ischemic stroke, assessing how these conditions interact and affect patient outcomes. By collecting clinical, laboratory, and imaging data, the study seeks to develop risk stratification and prognostic models, as well as to propose effective diagnostic and therapeutic strategies over a follow-up period of approximately three years.

Who should consider this trial

Good fit: Ideal candidates include adults aged 18 and older who have experienced an acute ischemic stroke and can provide informed consent.

Not a fit: Patients who are pregnant, breastfeeding, or participating in other interventional studies may not benefit from this research.

Why it matters

Potential benefit: If successful, this study could improve the understanding of heart-related complications in stroke patients, leading to better management and outcomes.

How similar studies have performed: While the interactions between heart diseases and acute ischemic stroke are recognized, this specific observational approach is relatively novel and has not been extensively tested in prior studies.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Written informed consent by patient
2. Age ≥ 18 years
3. Acute ischemic stroke (with matching brain lesion on MR imaging)
4. Enrolment within 24 h after onset of stroke-related symptoms.

Exclusion Criteria:

1. Pregnancy and / or breast-feeding.
2. Participation in an interventional study.
3. Patients refuse to participate in the research.

Where this trial is running

Suzhou, Jiangsu

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.

View on ClinicalTrials.gov →

Conditions: Acute Ischemic Stroke, Acute ischemic stroke, heart, Reperfusion Therapy

Last reviewed 2026-05-15 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.