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Thromboelastometry in Liver Transplantation

Transfusion Prediction Model in Orthotopic Liver Transplantation Based on Thromboelastometry: Prospective Validation Study.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03011827
Enrollment
65
Registered
2017-01-05
Start date
2019-08-01
Completion date
2022-10-31
Last updated
2019-08-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coagulopathy, Liver Transplant Disorder

Brief summary

Thromboelastometry better assess coagulation than standard coagulation test in patients undergoing ortothopic liver transplantation. In a post-hoc analysis from a randomized study recently conducted by our group, presurgical values of MA10 Extem \< 35 mm are highly predictive of RBC administration , with no further improvement over MA10 Extem \>40 mm ; suggesting that MA10 Extem between 35-40 would be the optimal range to manage blood product administration. The aim of the study is to validate this result in a prospective cohort of patients submitted to ortothopic liver transplantation.

Interventions

OTHERFibrinogen and/or platelets administration

Fibrinogen and/or platelets administration to maintain clot amplitude at 10 minutes of the thromboelastometry between 35-40 mm along liver transplant procedure

Sponsors

Hospital Clinic of Barcelona
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Presurgical hemoglobin \< 13 d/L and clot firmness at 10 minutes Extem \< 35 mm

Exclusion criteria

* Previous thrombosis * Antithrombotic treatment * No consent

Design outcomes

Primary

MeasureTime frame
Red blood cell transfusionuntil 24h after liver transplant

Secondary

MeasureTime frameDescription
Thrombosis28 days after liver transplantThrombosis will be assessed clinically and confirmed by ultrasonographic exam

Countries

Spain

Contacts

Primary ContactAnnabel Blasi, MD, PhD
ablasi@clinic.ub.es+34679500857

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026