Acute CoROnary Syndrome, Stroke and Sleep

Acute CoROnary Syndrome, Stroke and Sleep - ACROSSS

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00013559

Enrollment

328

Registered

2018-06-21

Start date

2018-07-01

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

I21 I63

Interventions

Group 1: The ACROSSS Study includes patients who have sufferred from a myocardial infarction, a stroke or a transient ischemic attack. The aim of the study is to answer two questions: First, to invest

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria for patients with myocardial infarction: first event (STEMI or NSTEMI), percutanous coronary intervention; no valvular defect Inclusion criteria for patients with stroke: first stroke ever; all transient ischemic attacks (not only first events)

Exclusion criteria

Exclusion criteria: no ability of giving consent; aphasia, dementia, confusion of the patient; for incidence study only: place of residences out of Essen and surrounding area

Design outcomes

Primary

Measure	Time frame
incident daytime napping; incident sleep disturbances; trigger of acute myocardial infarction / of stroke	—

Secondary

Measure	Time frame
Mortality	—

Countries

Germany

Contacts

Public ContactAnna-Therese Lehnich

Institut für Medizinische Informatik, Biometrie und Epidemiologie

acrosss@uk-essen.de0201 92239 289

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026