Liver Cancer Trial, Recruiting NCT05887661 Sponsor: The First Affiliated Hospital with Nanjing Medical University Condition: Liver Cancer
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Liver Cancer Trial, Recruiting

NCT05887661
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have been clinically diagnosed with hepatocellular carcinoma (a type of liver cancer)
  • People for whom laparoscopic hepatectomy (keyhole surgery to remove part of the liver) has been chosen as the surgical approach, and who agree to take part

Who may not be able to join:

  • People under 18 years of age
  • People who are pregnant
  • People who decline to receive blood product transfusions if needed
  • People with active heart problems, such as unstable chest pain, poorly controlled heart failure, serious irregular heartbeat, severe heart valve disease, or a history of congestive heart failure
  • People with a significant history of stroke or other cerebrovascular (brain blood vessel) disease
  • People with lung conditions that restrict or block normal breathing
  • People with high blood pressure that is not well controlled
  • People with reduced kidney function, specifically a filtration rate below 60 mL/min (confirm with trial site)
  • People with a low haemoglobin level (below 100 g/L), which may indicate anaemia
  • People with abnormal blood clotting results, including a clotting measure (INR) above 1.5 when not on warfarin, and/or a low platelet count below 100 ×10⁹/L
  • People with signs of a liver processing disorder, specifically elevated bilirubin above 35 mmol/L (confirm with trial site)
  • People with an active infection at the time of the trial
  • People who have donated their own blood before the operation (preoperative autologous blood donation)
  • People who have received the drug erythropoietin at any point during their hospital stay for this procedure

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 21 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Shijiang Liu, MD, The First Affiliated Hospital with Nanjing Medical University

Phone: +862568303569

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
1 May 2022
Est. completion
1 January 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

The proportion of allogeneic red blood cell products transfusion

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov