Actively Recruiting

Phase Not Applicable
Age: 18Years - 99Years
All Genders
NCT05355909

High Intensity PreHab Before Major Abdominal Surgery

Led by Medical University Innsbruck · Updated on 2025-03-26

60

Participants Needed

1

Research Sites

230 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The risk for major cardiac cardiovascular events (MACE) within the first 30 day after surgery is nit only associated to the patient relate risk factors but also to the kind of surgery. Surgical interventions can be distinguished infield risk (MACE \<1%), moderate risk (MACE 1-5%) and high risk (MACE \> 5%). In addition with patient related risk factors it can raise to values of 40%. The preoperative aerobic fitness \[oxygen uptake (VO2) at the ventilatory anaerobic threshold (VAT) \<11 mL/kg/min\] has been shown of particularly interest in identifying patients at increased risk of postoperative complications. In the last decade major interest was put in the question whether a preoperative personalised physical training may have beneficial effect on the preoperative fitness and on the occurrence of postoperative complications. In some small studies this benefit has been shown for abdominal and thoracic surgery. However some of those studies are controversially discussed because of missing randomisation and methodical issues. Also most of the studies needs a four week training period. This may lead to ethical and logostical problems oncologic patients. The aim of this study is to assess the effect of a personalised, high intensity trains program of two weeks on the preoperative fitness.

CONDITIONS

Official Title

High Intensity PreHab Before Major Abdominal Surgery

Who Can Participate

Age: 18Years - 99Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • ASA I-III
  • Body mass index (BMI) between 18 and 35 kg/m2
  • Signed informed consent
  • Scheduled for elective abdominal surgery with moderate to high risk
Not Eligible

You will not qualify if you...

  • Pregnancy or breastfeeding
  • Major trauma or massive hemorrhage within the last two weeks
  • Participation in another interventional study
  • Contraindication for preoperative fitness training or ergometry
  • Undergoing transplantation surgery

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 Hospital

Innsbruck, Tyrol, Austria, 6020

Actively Recruiting

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Research Team

L

Lukas Gasteiger, MD, PD

CONTACT

H

Helmut Raab, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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High Intensity PreHab Before Major Abdominal Surgery | DecenTrialz