Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- Patients scheduled for liver resection surgery
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
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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