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CompletedNCT05164406Updated May 31, 2023

Impact of Blood Salvage Therapy on Outcomes After Oncologic Liver Surgery

An observational study in Liver Neoplasms, sponsored by Université de Sherbrooke. Completed at 1 site in Canada. Open to participants aged 18 Years to 100 Years. Per ClinicalTrials.gov, last updated 2023-05-31.

Sponsored by Université de Sherbrooke · Observational

Study type
Observational
Model
Case-control
Time perspective
Retrospective
Enrollment
106
Ages
18 Years to 100 Years
Sex
All
01

Study summary

A before and after trial comparing the systematic use of blood salvage therapy with leucocyte filter during oncologic liver resections. Recurrence, survival, allogenic transfusion rates and surgical outcomes are compared with a representative historic cohort.

Read the detailed description

Blood salvage therapy in oncologic liver surgery is seldom used based on unproven concerns about the safety of the technique regarding potential cancer dissemination or recurrence. Nevertheless, the technique has proven advantages in other surgical settings regarding the allogenic transfusion outcomes. Allogenic blood transfusion has been scientifically proven to worsen prognosis in oncologic surgery. This study compares a cohort of patients systematically exposed the blood salvage therapy to one comparable cohort without the therapy and outcomes regarding transfusion rates, post-operative Hb measurement, recurrence, overall survival, and post-operative adverse events.

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Conditions studied

  • Liver Neoplasms

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Keywords

  • Blood salvage therapy
  • Oncologic liver surgery
03

In context

Liver Neoplasms

1,391 studies on the registry are indexed under Liver Neoplasms; 345 are open to participants now.

This study's enrollment of 106 is below the median of 200 across 350 observational studies indexed under Liver Neoplasms.

Browse Liver Neoplasms studies →

Lead sponsor

Université de Sherbrooke is the lead sponsor of 289 studies on the registry; 68 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 100 Years
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Adults undergoing liver surgery for any cancer in our institution between january 2018 and August 2019 (blood salvage group) and patients who underwent liver surgery without blood salvage between 2011 and 2018 (control group)

Inclusion criteria

  • Adult Oncologic liver surgery scheduled in our institution

Exclusion criteria

Exclusion Criteria:

  • Condition precluding consent for trial Pregnancy
05

Study design

Observational model
Case-control
Time perspective
Retrospective
Enrollment
106 participants (actual)
Patient registry
No

Groups and cohorts

  • With blood salvage

    Patients undergoing oncologic liver surgery with systematic use of blood salvage therapy

    Procedure: Blood salvage therapy

  • Without blood salvage

    Patients undergoing oncologic liver surgery without any blood salvage therapy

Interventions

  • ProcedureBlood salvage therapy

    In the blood salvage group, blood is systematically given back when the minimal amount of blood loss required for reprocessing is met

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What researchers measure

Primary outcomes

  1. Recurrence free survival

    Time frame: 18 months

  2. Overall survival

    Time frame: 18 months

  3. Transfusion

    Allogenic blood products requirements

    Time frame: Up to 30 days after surgery

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Study locations

1 site
  • Centre Hospitalier Universitaire de Sherbrooke
    Sherbrooke, Quebec J1G5N3, Canada
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 31, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05164406
Lead sponsor
Université de Sherbrooke
Responsible party
Sponsor
First posted
Dec 20, 2021
Start date
Jan 1, 2018
Primary completion
Aug 1, 2019
Completion
Feb 28, 2021
Last update
May 31, 2023

Study contacts

Yves Collin, MD
principal investigator · Université de Sherbrooke

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2023. You cannot join it, but the record below documents what was studied.

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