Utility of ROTEM® for Risk Stratification of Post-Invasive Procedure Hemorrhage in Patients With Cirrhosis (CIR-ROTEM)

Recruiting Observational Study
Cirrhosis, Liver
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 – 65
Sex
Any
Study type
Observational
Participants needed
330 (estimated)
Sponsor
Instituto de Investigación Marqués de Valdecilla · Other
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About This Trial
The assessment of post-procedural bleeding risk in cirrhosis remains a clinical challenge due to the lack of precise predictive tools and its high associated mortality. Although guidelines recommend a restrictive transfusion policy, adherence remains low, with a high rate of prophylactic transfusions despite unclear benefits. This multicenter, prospective, and observational study will evaluate the…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age between 18 and 85 years. * Clinical, analytical, elastographic, histological, and/or imaging criteria consistent with the diagnosis of hepatic cirrhosis. * Undergoing a high-risk invasive procedure, either in an outpatient setting or during hospitalization. * Platelet coun…
Contacts

jose ignacio fortea

942202520

jifortea@gmail.com

CONTACT