Managing bleeding during liver transplantation

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study focuses on the management of hemostasis during liver transplantation, a procedure associated with significant bleeding risks. It aims to identify and analyze various risk factors that contribute to intraoperative bleeding and transfusion needs, which can occur at different phases of the surgery. By examining patient characteristics and surgical phases, the study seeks to improve predictive models for transfusion requirements, ultimately enhancing patient outcomes during liver transplantation.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patients aged 18 or over
* Liver transplant patient

Exclusion Criteria:

* Multi-organ transplantation
* Protected populations: under guardianship or curatorship
* Patients not affiliated to a social security scheme

Where it's running

• Chru Minjoz
  Besançon, France Recruiting
• CHU Claude Huriez
  Lille, France Recruiting
• Hôpital de la Croix-Rousse
  Lyon, France Recruiting
• Hôpital Paul Brousse
  Villejuif, France Recruiting
• CHU Estaing
  Clermont, France Not yet recruiting
• Hôpital Beaujon
  Clichy, France Not yet recruiting

Study contacts

• Principal investigator: Weiss, Md — Hôpital Beaujon
• Study coordinator: Emmanuel WEISS, MD
• Email: emmanuel.weiss@aphp.fr
• Phone: +33 1 40 87 58 81

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.