Actively Recruiting

Phase 4
Age: 18Years +
All Genders
NCT04731558

Pre- Vs Postoperative Thromboprophylaxis for Liver Resection

Led by Helsinki University Central Hospital · Updated on 2025-02-14

1012

Participants Needed

7

Research Sites

315 weeks

Total Duration

On this page

Sponsors

H

Helsinki University Central Hospital

Lead Sponsor

A

Academy of Finland

Collaborating Sponsor

AI-Summary

What this Trial Is About

Thromboprophylaxis for liver surgery can be commenced either preoperatively or postoperatively. Despite a clear trade-off between thrombosis and bleeding in liver surgery patients, there is no international consensus when thrombosis prophylaxis should be commenced in patients undergoing liver surgery. As far as we know, there are no prospective randomized trials in this field, and current guidelines are unfortunately based on very low quality evidence, that is, a few retrospective studies and expert opinion. Both American and European thromboprophylaxis guidelines for abdominal cancer surgery support the preoperative initiation of thromboprophylaxis, but these guidelines do not specifically address the increased bleeding risk associated with liver surgery. On the contrary, Dutch guidelines recommend postoperative thromboprophylaxis only, because of lack of evidence for preoperative thromboprophylaxis. Traditionally, many liver surgery units have been reluctant in using preoperative thromboprophylaxis due to the potentially increased risk of bleeding complications. Enhanced Recovery After Surgery (ERAS) Society Guidelines recommend preoperative thromboprophylaxis in liver surgery, but the guidelines provide no supporting evidence for this recommendation. Overall, the amount of evidence is scarce and somewhat contradictory in this clinically relevant field of thromboprophylaxis in liver surgery. The aim of this study is to compare pre- and postoperatively initiated thromboprophylaxis regimens in liver surgery in a randomized controlled trial.

CONDITIONS

Official Title

Pre- Vs Postoperative Thromboprophylaxis for Liver Resection

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients scheduled for liver resection surgery
Not Eligible

You will not qualify if you...

  • Use of anticoagulant medication (heparin, low-molecular weight heparin, warfarin, or direct oral anticoagulants) within one month before surgery
  • Emergency liver surgery due to trauma or infection
  • Age under 18 years
  • Allergy or contraindication to planned low-molecular weight heparin
  • Unable to provide written informed consent
  • Liver resection not performed after randomization

AI-Screening

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Trial Site Locations

Total: 7 locations

1

Helsinki University Hospital

Helsinki, Finland

Actively Recruiting

2

Kuopio University Hospital

Kuopio, Finland

Actively Recruiting

3

Oulu University Hospital

Oulu, Finland

Not Yet Recruiting

4

Tampere University Hospital

Tampere, Finland

Actively Recruiting

5

Turku University Hospital

Turku, Finland

Not Yet Recruiting

6

Oslo University Hospital

Oslo, Norway

Actively Recruiting

7

University Hospital of North Norway

Tromsø, Norway

Actively Recruiting

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Research Team

V

Ville Sallinen, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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Pre- Vs Postoperative Thromboprophylaxis for Liver Resection | DecenTrialz