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Peri-Operative Measurement Of NT-ProBNP To Predict Outcomes In Patients Undergoing Elective Vascular Surgery

Colney
Posted about 1 month ago
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Age: 18 Years +

All Genders

ID: 04014647

Peri-operative Measurement of NT-proBNP to Predict Outcomes in Patients Undergoing Elective Vascular Surgery

Led by: Norfolk and Norwich University Hospitals NHS Foundation Trust

Updated on: 2026-06-08

200 Participants Needed

1 Research Site

Total Duration: N/A

On this page

  • AI-Summary
  • Brief Title
  • Who Can Participate
  • AI-Screening
  • Your Study Journey
  • Trial Site Locations
  • Research Team
  • How is the study designed?
  • Similar Trials
  • Frequently Asked Questions
  • Research Publications

AI-Summary

What This Trial Is About

Researchers are evaluating whether measuring N-terminal pro B-type natriuretic peptide NT-proBNP and other heart-related markers can help predict outcomes for patients undergoing elective major vascular surgery. The study aims to identify high-risk patients who may face serious complications like heart attacks or death after surgery. Understanding these risks could help guide treatments to improve patient care and long-term health. This observational study measures NT-proBNP levels before and four days after surgery. It also tracks other markers such as troponin I, galectin-3, CRP, and creatinine during the same peri-operative period. Patients are grouped based on whether they experience negative events post-surgery, including cardiac events, infections, kidney issues, or extended hospital stays. Participants will have blood tests at specified times around surgery and be monitored for various clinical events within 31 days after surgery. The study collects data on hospital stay length, use of antibiotics, inotropic support, and kidney alerts. Researchers aim to use these measurements to better predict patient outcomes and potentially guide future interventions for improved recovery and survival.

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CONDITIONS

Brief Title

Measurement Of NT-proBNP to Predict Outcomes in Surgery

Who Can Participate

Age: 18 Years +

All Genders

Eligibility Criteria

You may qualify if you...

  • Patients who are equal to or over 18 years old
  • Patients scheduled to undergo elective surgery for infrainguinal arterial reconstruction
  • Patients scheduled to undergo elective surgery for aortic aneurysm
  • Patients scheduled to undergo elective surgery for aorto-bifemoral bypass or aortic endarterectomy
  • Patients scheduled to undergo elective surgery for femoro-popliteal bypass
  • Patients scheduled to undergo elective surgery for femoro-distal bypass
  • Patients scheduled to undergo elective surgery for femoral endarterectomy
  • Patients scheduled to undergo elective surgery for femoro-femoral crossover
  • Patients scheduled to undergo elective surgery for axillo-femoral bypass
  • Patients scheduled to undergo elective carotid surgery
  • Patients having either general or regional anaesthesia for their surgery

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You will not qualify if you...

  • Patients undergoing emergency surgery
  • Patients unable or unwilling to give informed consent
  • Patients with unstable coronary syndromes including recent myocardial infarction or severe angina
  • Patients with decompensated heart failure with new or worsening symptoms
  • Patients with chronic atrial fibrillation

Research Team

  • E: Emma Miler, MSc BSc Hons
  • A: Allison Chipchase, Dr

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Sponsors

N: Norfolk and Norwich University Hospitals NHS Foundation Trust

Lead Sponsor: Norfolk and Norwich University Hospitals NHS Foundation Trust

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Skills

Clinical Research
Patient Monitoring
Blood Sampling
Data Collection
Peri-operative Care
Vascular Surgery Knowledge

Location

Colney, England, United Kingdom

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