Perioperative Management & Outcome Following Preoperative Transthoracic Echocardiography in Noncardiac Surgery Patients
NCT ID: NCT06409234
Last Updated: 2024-05-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
8250 participants
OBSERVATIONAL
2024-06-30
2026-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Exposed group
5500 exposed group will be patients in whom Transthoracic Echocardiography was performed within 3 months before surgery. Controls will be patients in whom Transthoracic Echocardiography was NOT performed.
Transthoracic Echocardiography Recieved
Transthoracic Echocardiography Recieved
Interventions
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Transthoracic Echocardiography Recieved
Transthoracic Echocardiography Recieved
Eligibility Criteria
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Inclusion Criteria
* above 18 years and presenting ≥2 cardiovascular risk factors (hypertension, smoking, dyslipidaemia, diabetes, family history of CVD) OR
* above 18 years with known cardiovascular disease
Exclusion Criteria
* day surgery
* urgent/emergency procedures
* current ICU patient (i.e. in ICU on day-1 or the day of the index surgery (day 0)),
* cardiac surgery within the last month prior according to the index noncardiac procedure (of note this does not include cardiological interventions like TAVI or valvuloplasty),
* unwilling or unable to provide informed consent,
* unable to complete the WHODAS questionnaire (literacy or language barrier)
* Previous enrollment in EuPreCHO (in case of repeated surgery)
18 Years
ALL
No
Sponsors
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European Society of Anaesthesiology
OTHER
Responsible Party
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Principal Investigators
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Giovanna Lurati Buse, Prof
Role: PRINCIPAL_INVESTIGATOR
Heinrich-Heine University, Duesseldorf
Locations
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University Hospital Düsseldorf
Düsseldorf, , Germany
Countries
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Central Contacts
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Other Identifiers
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EuPreCHO
Identifier Type: -
Identifier Source: org_study_id
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