- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07634822
Heart Failure and Postoperative Outcome in Surgery - a National Registry Study
June 2, 2026 updated by: Umeå University
Incidence of Heart Failure and Its Association With Postoperative Mortality in Surgery - a National Registry Study
The study is an exploratory study that aims to explore the incidence of heart failure in a national surgical cohort, and to compare postoperative mortality and morbidity in patients with and without heart failure.
Furthermore, we want to investigate differences in the incidence of heart failure and its impact on postoperative morbidity and mortality in day surgery compared to inpatient surgery.
Study Overview
Status
Not yet recruiting
Study Type
Observational
Enrollment (Estimated)
2200000
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
- Name: Tomi Myrberg, Associate professor
- Phone Number: +46920282236
- Email: tomi.myrberg@umu.se
Study Locations
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-
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Luleå, Sweden
- Region Norrbotten, department of Anesthesia and Intensive Care, Sunderby Hospital
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Principal Investigator:
- Tomi Myrberg, Associate professor
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Umeå, Sweden
- Institution for Diagnostic and Intervention, dep of Anestesiology and Intensive care
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Contact:
- Tomi Myrberg, Associate professor
- Phone Number: +46920282236
- Email: tomi.myrberg@umu.se
-
Principal Investigator:
- Tomi Myrberg, Associate professor
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients ≥18 years of age who underwent surgery in Sweden between 1 Jan 2021-31 Dec 2024.
Description
Inclusion Criteria:
- ≥18 years of age who underwent surgery in Sweden between 1 Jan 2021-31 Dec 2024 and SPOR registered operation.
Exclusion Criteria:
- ASA 6 (deceased patient, organ donation).
- Cardiac surgery
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
Cohorts and Interventions
Group / Cohort |
|---|
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Surgery with SPOR registration
Surgery registered in SPOR registry between 2021--2024
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Postoperative mortality
Time Frame: 365 days
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How does a heart failure diagnosis affect postoperative mortality at 30 days, 90 days, 180 days, and 365 days?
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365 days
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Postoperative morbidity
Time Frame: 30 days postoperative
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How does a heart failure diagnosis associated with postoperative morbidity at 30 days?
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30 days postoperative
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Prevalence of heart failure
Time Frame: 5 years preoperative
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What is prevalence of heart failure in surgery in Sweden?
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5 years preoperative
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Differences between ambulatory and inpatient surgery
Time Frame: 365 postoperative
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Is there difference between ambulatory respective elective surgery regarding mortality and morbidity after surgery?
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365 postoperative
|
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Difference in prevalence of heart failure
Time Frame: 5 years preoperative
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Is there difference in prevalence regarding ambulatory and inpatient surgery
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5 years preoperative
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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
- 1. Griffiths R, Beech F, Brown A, Dhesi J, Foo I, Goodall J, et al. Peri-operative care of the elderly 2014: Association of Anaesthetists of Great Britain and Ireland. Anaesthesia. 2014;69 Suppl 1:81-98. 2. Weiser TG, Haynes AB, Molina G, Lipsitz SR, Esquivel MM, Uribe-Leitz T, et al. Estimate of the global volume of surgery in 2012: an assessment supporting improved health outcomes. Lancet. 2015;385 Suppl 2:S11. 3. Eriksson J, Sandberg C, Kilhamn N, Bell M, Oldner A, Larsson E. Surgery in patients aged ≥ 80 years: mortality and recovery in a nationwide cohort study. Anaesthesia. 2025;80(7):812-22. 4. McDonagh TA, Metra M, Adamo M, Gardner RS, Baumbach A, Böhm M, et al. 2021 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure: Developed by the Task Force for the diagnosis and treatment of acute and chronic heart failure of the European Society of Cardiology (ESC). With the special contribution of the Heart Failure Association (HFA) of the ESC. European journal of heart failure. 2022;24(1):4-131. 5. Lindberg F, Benson L, Dahlström U, Lund LH, Savarese G. Trends in Heart Failure Mortality in Sweden Between 1997 and 2022. European journal of heart failure. 2024;27(2):366-76. 6. Shah KS, Xu H, Matsouaka RA, Bhatt DL, Heidenreich PA, Hernandez AF, et al. Heart Failure With Preserved, Borderline, and Reduced Ejection Fraction: 5-Year Outcomes. J Am Coll Cardiol. 2017;70(20):2476-86. 7. Levy D, Kenchaiah S, Larson MG, Benjamin EJ, Kupka MJ, Ho KK, et al. Long-term trends in the incidence of and survival with heart failure. N Engl J Med. 2002;347(18):1397-402. 8. Hernandez AF, Whellan DJ, Stroud S, Sun JL, O'Connor CM, Jollis JG. Outcomes in heart failure patients after major noncardiac surgery. J Am Coll Cardiol. 2004;44(7):1446-53. 9. van Diepen S, Bakal JA, McAlister FA, Ezekowitz JA. Mortality and Readmission of Patients With Heart Failure, Atrial Fibrillation, or Coronary Artery Disease Undergoing Noncardiac Surgery. Circulation. 2011;124
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 (Estimated)
August 1, 2026
Primary Completion (Estimated)
March 1, 2027
Study Completion (Estimated)
December 1, 2030
Study Registration Dates
First Submitted
June 2, 2026
First Submitted That Met QC Criteria
June 2, 2026
First Posted (Actual)
June 9, 2026
Study Record Updates
Last Update Posted (Actual)
June 9, 2026
Last Update Submitted That Met QC Criteria
June 2, 2026
Last Verified
June 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Dnr 2026-01286-01
- 36223/2026 (Registry Identifier: National Cause of Death Register, Sweden)
- DAT-1428 (Other Identifier: The Swedish Perioperative Registry (SPOR))
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Not actual in this study concept
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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