Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07391683

Telemedically Assisted Optimization for Heart Failure Patients Before Cardiac Surgery to Improve Perioperative Outcome

Led by Medical University Innsbruck · Updated on 2026-02-18

162

Participants Needed

1

Research Sites

410 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Patients with heart failure undergoing cardiac surgery face a significantly increased perioperative risk, yet no standardized strategy exists to mitigate this risk effectively. Current preoperative management relies on optimization of medical therapy without a structured prehabilitation approach. Given the strong association between eleveated preoperative N-terminal pro-B-type natriuretic peptide levels and postoperative outcomes, patients at increased risk could be identified using this biomarker. Telemedical disease management programs have demonstrated efficacy in outpatient heart failure care, but their role in preoperative optimization remains underexplored. This study aims to assess whether a structured, multidisciplinary, telemedicine-assisted prehabilitation program can reduce perioperative complications, and improve surgical outcomes.

CONDITIONS

Official Title

Telemedically Assisted Optimization for Heart Failure Patients Before Cardiac Surgery to Improve Perioperative Outcome

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Indication for elective cardiac surgery in the Heart team
  • NTproBNP 6 1500 ng/L
  • 18 years or older and willing to participate in trial
  • Written informed consent
Not Eligible

You will not qualify if you...

  • Neuropsychiatric disorders or illnesses (e.g., drug addiction, alcohol abuse) that prevent adherence to the study
  • Insufficient ability to measure and transfer data or lack of social support
  • Insufficient ability to communicate (language skills, eyesight, hearing)
  • Pregnancy
  • Chronic kidney disease requiring dialysis
  • Planned procedures including heart transplantation or left ventricular mechanical assist device implant

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Medical University of Innsbruck - Department of Cardiology & Department of Cardiac Surgery

Innsbruck, Tyrol, Austria, 6020

Actively Recruiting

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Research Team

C

Can Gollmann-Tepeköylü, Prof.

CONTACT

L

Leo Winter-Pölzl, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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