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Myocardial Damage In Patients With Cerebral Infarction

Myocardial Damage In Patients With Cerebral Infarction. Prevalence and Characteristics as Measured by Troponins, Electrocardiographic Changes and Myocardial Perfusion Imaging.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00306579
Enrollment
250
Registered
2006-03-24
Start date
2003-08-31
Completion date
2005-05-31
Last updated
2017-08-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ischemic Stroke

Keywords

Ischemic Stroke, Myocardial ischemia, Myocardial necrosis

Brief summary

Introduction For several years ischemic electrocardiographic (ECG) changes in the acute phase of ischemic stroke have been reported. Whether these ECG changes reflect true myocardial ischemia remains controversial. So far no study has assessed different markers of myocardial ischemia or necrosis in consecutive patients admitted to hospital with an acute ischemic stroke. Purpose The main purpose of this study is to determine the potential burden of reversible and irreversible myocardial ischemia in patients with an acute ischemic stroke. Patients and methods Serial blood samples for measuring troponin T, CK-MB and NT-proBNP are collected in 250 patients with evidence of an acute ischemic stroke admitted to the Department of Neurology at Odense University Hospital. In addition resting 12-lead ECG recordings will be obtained on a daily basis, and a 24-hour ST-segment ambulatory monitoring will be performed once within the first week of hospitalisation. Finally, myocardial perfusion patterns during rest will be evaluated by means of a myocardial perfusion scintigraphy in patients with an elevated troponin T level. Six months later control measurements of troponin T, CK-MB and NT-proBNP and a 12-lead ECG will be obtained. Expectations The study will contribute with original observations in patients with acute ischemic stroke considering the following issues: 1. The prevalence and characteristics of ECG changes suggestive of myocardial ischemia. 2. The prevalence of transient ST-segment changes on ambulatory monitoring. 3. The prevalence and degree of myocardial necrosis as judged from biochemical markers. 4. The prevalence of reversible and irreversible perfusion defects on myocardial scintigraphy. 5. The prevalence, size and patterns of NT-proBNP. 6. Whether there is a change in ECG and biochemical markers over a 6-month follow-up period. The results may have clinical implications regarding early and late treatment as well as clinical follow-up of patients recovering from an episode of acute ischemic stroke.

Interventions

None listed

Sponsors

Fonden for Lægevidenskabelig Forskning for Fyns Amt.
CollaboratorUNKNOWN
Novo Nordisk A/S
CollaboratorINDUSTRY
AJ Andersen og Hustrus Fond
CollaboratorOTHER
Overlægerådet Legatudvalg
CollaboratorUNKNOWN
Raimond and Dagmar Ringgård-Bohn's Foundation
CollaboratorOTHER
Bankdirektør Hans Stener og hustru Agnes Steners legat
CollaboratorUNKNOWN
Odense University Hospital
CollaboratorOTHER
Danish Heart Foundation
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Acute ischemic stroke. 2. Age ≥ 18 years old. 3. Written, informed consent.

Exclusion criteria

1. Onset of stroke symptoms 8 to 21 days before admission. 2. Transient ischemic attack. 3. Intracerebral or subarachnoid haemorrhage. 4. Previous myocardial infarction. 5. Any pathological Q waves on the baseline ECG. 6. Current atrial fibrillation. 7. Unstable angina pectoris ≤ 3 weeks before admission. 8. Systolic blood pressure ≤ 90 mmHg and symptoms. 9. Resuscitation after cardiac arrest. 10. Unwillingness to participate.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026