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Clinical Trials/NCT04769752
NCT04769752
Completed
Not Applicable

Use and Prescription of Beta-blockers Before Cardiac Surgery With Cardiopulmopnary Bypass: Multicenter Observational Analysis of Practices and Its Association With Postoperative Morbidity-mortality.

Centre Hospitalier Universitaire Dijon1 site in 1 country1,789 target enrollmentJune 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiac Surgery With Cardiopulmonary Bypass
Sponsor
Centre Hospitalier Universitaire Dijon
Enrollment
1789
Locations
1
Primary Endpoint
Number of patients treated with beta-blocker in accordance with international guidelines
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The objective of this study is to describe in a cohort of cardiac surgery patients the use of beta-blockers before surgery and their maintenance or withdraw according to international recommendations in order to compare patients who receive a beta-blocker with maintenance during the surgical period (international recommendation) to those for whom prescription and maintenance are not respected. Patients are treated according to standard practice and this protocol does not change patient management. No additional information or data is required by the study other than the data usually collected in the patient record (drug treatment, medical history, operating data, postoperative data, complications, length of stay).

The objectives of this research are :

  • To evaluate the proportion of patients receiving beta-blocker treatment prior to cardiac surgery.
  • To evaluate the proportion of patients receiving beta-blocker treatment before cardiac surgery and complying with international recommendations for its maintenance/stop in perioperative cardiac surgery.
  • To evaluate the incidence of complications and length of hospital stay in patients receiving beta-blockers based on compliance or non-compliance with recommendations.
Registry
clinicaltrials.gov
Start Date
June 2020
End Date
December 22, 2023
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Major patient ≥ 18 years
  • Patient operated cardiac surgery with cardiopulmonary bypass
  • Patients who have given oral consent to participate after full information

Exclusion Criteria

  • Off pump cardiac surgery

Outcomes

Primary Outcomes

Number of patients treated with beta-blocker in accordance with international guidelines

Time Frame: 7 days

Number of patients treated with beta-blocker in accordance with international guidelines

Study Sites (1)

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