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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05225246
Other study ID # 2020-02023; kt22Reuthebuch
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 1, 2020
Est. completion date December 31, 2021

Study information

Verified date January 2022
Source University Hospital, Basel, Switzerland
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to analyze the reasons for unplanned readmissions after cardiac surgery at the University Hospital Basel. Predictive factors for readmissions and the development over the last 10 years will be analyzed.


Recruitment information / eligibility

Status Completed
Enrollment 4882
Est. completion date December 31, 2021
Est. primary completion date December 31, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria for readmission group: - Patients who had heart surgery and returned unplanned to the University Hospital Basel within 30 days of leaving the hospital (outpatient or inpatient) Inclusion Criteria for control group: - Patients who had heart surgery and did not return unplanned to the University Hospital Basel within 30 days of leaving the hospital (outpatient or inpatient) Exclusion Criteria: - Patients with other initial hospitalization reasons for heart surgery without heart surgery (conservative treatments, cerclage removal, pacemaker surgery) are not included in the analysis. - Planned readmissions to the University Hospital Basel within 30 days

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Data collection on reasons for unplanned readmission to the University Hospital Basel within 30 days of leaving the hospital
Descriptive analysis of the reasons for unplanned readmissions after cardiac surgery and predictive factors for unplanned readmissions and validation of risk scores

Locations

Country Name City State
Switzerland University Hospital Basel, Cardiac Surgery Clinic Basel

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Basel, Switzerland

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of cardiac related readmissions compared to infections, bleedings and neurological causes Number of cardiac related readmissions compared to infections, bleedings and neurological causes one time assessment at baseline
Primary Sex specific reasons for readmissions Differences in sex specific reasons for readmissions one time assessment at baseline
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