SURgical Registry of ENDocarditis EuRope (SURRENDER)

May 9, 2023 updated by: Matthias Thielmann, University Hospital, Essen

SURgical Registry of Infective ENDocarditis in EuRope - SURRENDER

This is a prospective, multicentric, european registry of patients with infective endocarditis undergoing cardiac surgery. Patient demographics, clinical data and laboratory values will be collected, as well as treatment outcomes at day 30, day 90 and 1-5 years after the intervention.

Study Overview

Status

Not yet recruiting

Intervention / Treatment

Detailed Description

Infective endocarditis (IE) is now a relatively rare but worldwide disease (3-10 IE/100000 population/year) with increasing incidence especially in the Western world. IE is still associated with high morbidity and mortality, prolonged hospital stay, high risk of reinfection, significantly worsened prognosis for patients, substantially reduced quality of life, and in any case represents a major financial burden for the respective healthcare systems [1-11].

Patients who need to undergo cardiac surgery due to infective endocarditis (IE) are heterogeneous and present with a persistently high perioperative morbidity and mortality rate. Despite optimal and individualized perioperative management strategies, perioperative complications such as heart failure, systemic inflammatory response, vasoplegia, and sepsis is still the main reason for adverse outcomes following cardiac surgery.

The present European, multicenter IE registry (Surgical RegistRy of infective ENDocarditis in EuRope - SURRENDER) was initiated and established to record and appropriately analyze current surgical treatment options and perioperative adjunctive treatment strategies, as well as short- and long-term patient outcomes.

Study Type

Observational

Enrollment (Anticipated)

10000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Essen, Germany, 45122
        • University Hospital Essen, Department of Thoracic and Cardiovascular Surgery, West-German Heart and Vascular Center, University Duisburg-Essen
        • Contact:
        • Contact:
        • Principal Investigator:
          • Matthias Thielmann, Prof.
    • Bavaria
      • Nürnberg, Bavaria, Germany, 90471
        • Department of Cardiac Surgery, Hospital Nürnberg, Paracelsus Medical University
        • Contact:
        • Principal Investigator:
          • Jurij Kalisnik, PD Dr.

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Patients with infective endocarditis undergoing open heart surgery with cardio-pulmonary bypass

Description

Inclusion Criteria:

  • Patients with infective endocarditis (according to DUKE criteria) undergoing cardiac surgery
  • Age ≥18 years
  • Written informed consent

Exclusion Criteria:

  • Age < 18 years
  • Missing declaration of consent
  • Current participation in another interventional trial

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: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
In-hospital mortality (all cause)
Time Frame: 30 days or during index hospitalization
Overall mortality rate in-hospital, at day 30 or during index hospitalization
30 days or during index hospitalization
Mortality at long-term follow-up
Time Frame: 1 to 5 years
at 1 to 5 years post-surgery
1 to 5 years

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
MACCE
Time Frame: 30 days or during index hospitalization

Major adverse cardiac and cerebrovascular event rate at day 30 or during index hospitalization.

Composite of 1.) Cardiac events: (postoperative myocardial infarction, CPR, LCOS/heart failure, repeat cardiac surgery) and/or cerebrovascular events (postoperative stroke, TIA, intracranial hemorrhage)

30 days or during index hospitalization
MACCE at long term follow-up
Time Frame: 1 to 5 years
Major adverse cardiac and cerebrovascular event rate at 1 to 5 years post-surgery
1 to 5 years
Sepsis accociated mortatilty
Time Frame: 30 days or during index hospitalization
Sepsis accociated mortatilty at day 30 or during index hospitalization
30 days or during index hospitalization
Post-operative sepsis
Time Frame: 30 days or during index hospitalization
Sepsis at day 30 or during index hospitalization
30 days or during index hospitalization
Vasoactive inotropic score
Time Frame: < 72h post-surgery
The sum of maximum dose rates of inotropes and/or vasopressor medications administered the first 72h post-surgery
< 72h post-surgery
Mechanical ventilation time
Time Frame: 30 days or during index hospitalization
Duration of postoperative invasive/mechanical ventilation post-surgery
30 days or during index hospitalization
Readmission due to IE recurrence
Time Frame: 30 days to 1 year post-surgery
Recurrence of infective endocarditis after 30 days to 1 year post-surgery
30 days to 1 year post-surgery
Renal failure
Time Frame: 30 days or during index hospitalization
Occurence of renal failure (KDIGO criteria)
30 days or during index hospitalization
Dialysis (RRT post-surgery)
Time Frame: 30 days or during index hospitalization
Occurence of renal failure requiring renal replacement therapy
30 days or during index hospitalization

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Matthias Thielmann, Prof. Dr., Department of Thoracic and Cardiovascular Surgery, University Hospital Essen
  • Principal Investigator: Jurij Kalisnik, PD. Dr., Department of Cardiac Surgery, Hospital Nürnberg, Paracelsus Medical University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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 (Anticipated)

September 1, 2023

Primary Completion (Anticipated)

December 1, 2032

Study Completion (Anticipated)

April 1, 2033

Study Registration Dates

First Submitted

September 28, 2022

First Submitted That Met QC Criteria

September 28, 2022

First Posted (Actual)

October 3, 2022

Study Record Updates

Last Update Posted (Actual)

May 10, 2023

Last Update Submitted That Met QC Criteria

May 9, 2023

Last Verified

May 1, 2023

More Information

Terms related to this study

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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