Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06882577

Heart Evaluation of Acute Ischemic Stroke With Reperfusion Therapy

Status
Recruiting
Phase
Study type
Observational
Enrollment
400 (estimated)
Sponsor
Soochow University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Heart Evaluation of Acute ischemic stroke with Reperfusion Therapy (HEART) is a single-center observational registry evaluating the heart of patients hospitalized for acute ischemic stroke with reperfusion therapy. This registry aims to establish quantified risk stratification and prognostic models, as well as suggest effective diagnostic and therapeutic strategies.

Detailed description

There is growing evidence pointing to close interactions between acute ischemic stroke (AIS) and heart diseases. Heart diseases may lead to AIS (heart-to-brain interactions), with many cardiac conditions have been proposed as potential sources of cerebral embolism, and studies have also shown that AIS can induce cardiac injury (brain-to-heart interactions), namely Stroke-Heart Syndrome. In addition, due to the commonly shared risk factors, AIS patients had a significantly higher frequency of coexisting prior known or unknown coronary heart disease (brain-and-heart interactions). These heart problems not only add complexity to the etiological diagnosis but also account for a great proportionate mortality in AIS patients with reperfusion therapy, which is the most effective treatment method for AIS. The interconnected and coexisting properties of AIS and heart diseases requires a comprehensive scheme to evaluate, prevent, and treat patients. Heart Evaluation of Acute ischemic stroke with Reperfusion Therapy (HEART) is a single-center observational registry evaluating the heart of patients hospitalized for acute ischemic stroke with reperfusion therapy. This registry aims to establish quantified risk stratification and prognostic models, as well as suggest effective diagnostic and therapeutic strategies. The clinical, laboratory and imaging information will be collected at the baseline. During an estimated 3-year follow-up, the diagnostic or monitoring procedures, treatment, functional status and new vascular events will be recorded by web-based patients' self-reports, investigators' regular telephone visits.

Conditions

Interventions

TypeNameDescription
OTHERobservational only- no interventionobservational only- no intervention

Timeline

Start date
2025-03-31
Primary completion
2026-03-31
Completion
2029-03-31
First posted
2025-03-18
Last updated
2025-05-13

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06882577. Inclusion in this directory is not an endorsement.