- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05225246
Readmissions After Cardiac Surgical Procedures
January 25, 2022 updated by: University Hospital, Basel, Switzerland
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.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
4882
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Basel, Switzerland, 4031
- University Hospital Basel, Cardiac Surgery Clinic
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
16 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Since January 2010, around 7,500 patients have had heart surgery, and around 2,083 of these patients have returned to the University Hospital of Basel within 30 days of discharge after heart surgery.
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Retrospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
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)
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Descriptive analysis of the reasons for unplanned readmissions after cardiac surgery and predictive factors for unplanned readmissions and validation of risk scores
|
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)
|
Descriptive analysis of the reasons for unplanned readmissions after cardiac surgery and predictive factors for unplanned readmissions and validation of risk scores
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of cardiac related readmissions compared to infections, bleedings and neurological causes
Time Frame: one time assessment at baseline
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Number of cardiac related readmissions compared to infections, bleedings and neurological causes
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one time assessment at baseline
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Sex specific reasons for readmissions
Time Frame: one time assessment at baseline
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Differences in sex specific reasons for readmissions
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one time assessment at baseline
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Oliver Reuthebuch, Prof. Dr. med., University Hospital Basel, Cardiac Surgery Clinic
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 1, 2020
Primary Completion (Actual)
December 31, 2021
Study Completion (Actual)
December 31, 2021
Study Registration Dates
First Submitted
January 25, 2022
First Submitted That Met QC Criteria
January 25, 2022
First Posted (Actual)
February 4, 2022
Study Record Updates
Last Update Posted (Actual)
February 4, 2022
Last Update Submitted That Met QC Criteria
January 25, 2022
Last Verified
January 1, 2022
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2020-02023; kt22Reuthebuch
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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