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Clinical Trials in Germany / NCT06409234
Starting soon Observational

Perioperative Management & Outcome Following Preoperative Transthoracic Echocardiography in Noncardiac Surgery Patients

NCT06409234 · tracked via the Priya Life Science Germany tracker
Sponsor
European Society of Anaesthesiology
Phase
Observational
Started
2024-06-30
Last updated
2024-05-10

Condition(s) studied

Elective Surgical Procedure

Investigational drug(s) / intervention(s)

Transthoracic Echocardiography Recieved

Transthoracic Echocardiography Recieved: Transthoracic Echocardiography Recieved

Study summary

In August 2022 the European Society of Cardiology published updated guidelines including recommendations on preoperative transthoracic echocardiography. The update resulted in broadened criteria for preoperative transthoracic echocardiography. The impact of preoperative transthoracic echocardiography on outcome is controversial and the evidence was mostly derived from administrative databases. Also there is also a knowledge gap in terms of what changes in perioperative managements are derived from transthoracic echocardiography information in current daily practice in Europe and what their impact on outcome may be. Further, a secondary analysis in a large international cohort suggests that the criteria endorsed by the guidelines to define the class of recommendation of transthoracic echocardiography may not be efficient.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria * aged ≥65 years OR * 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 * under 18 years of age * 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)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University Hospital Düsseldorf Düsseldorf Germany
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06409234 on ClinicalTrials.gov ↗ ← All trials in Germany