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OpenTrials
Completed

NCT Number: NCT04076605

Bleeding in Hospitalized Patients With Liver Disease Undergoing Invasive Procedures

Patients with cirrhosis are frequently hospitalized and often undergo procedures. Knowledge surrounding bleeding risk is sparse and practice patterns vary across centers in regards to bleeding prophylaxis. The goal of this study to is to obtain more knowledge regarding risk factors for procedural related bleeding in patients with cirrhosis and to develop a predictive model to risk stratify patients before undergoing procedures. Through collaboration from centers across the world this study should provide information on prevalence of bleeding and variation in practice patterns for prophylaxis.

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Key information

About this study

Hospitalized patients with cirrhosis who undergo 1 or more non-surgical procedure will be enrolled. The investigators will collect multiple clinical characteristics from the medical record and follow the patients prospectively over the hospitalization and/or until 28 days to determine if clinical events have occurred including bleeding, thrombosis, re-hospitalization and death. Characteristics of the hospitalization will be recorded including presence of acute decompensation and acute on chronic liver failure (ACLF). Procedure type will be recorded including coagulation laboratory data before and after each procedure. All bleeding events will be recorded and characteristics surrounding each bleed will be recorded. Bleeding will be defined according to International Thrombosis and Haemostasis (ISTH) definitions of major bleed and clinically relevant non-major bleed. REDCap (https://www.project-redcap.org) will be used to collect and centralize data maintained at the University of Virginia. Characteristics of each hospitalization will be recorded accordingly and patients will be followed for 28 days for outcome and mortality information. Each participating center will obtain local Institutional Review Board (IRB) approval to participate and enter data directly into REDCap. After center IRB approval is obtained, centers will consecutively enrolling patients on a rolling basis. Data will be collected from enrollment until death, transplant, discharge and/or 28 days on each individual enrolled.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patients with cirrhosis admitted to a hospital ward or ICU for greater than 24 hours.
  • Patient must undergo 1 or more invasive non-surgical procedures at admission or during the hospitalization.

Exclusion criteria

  • Age < 18 years old
  • Prisoner
  • Pregnant
  • Unable to provide consent
  • Previously enrolled in this study

Treatment and study plan

Primary outcomes

  1. Prevalence of procedural-related bleeding events in patients with cirrhosis

    Time frame: Each patient enrolled will be followed for 28 days

    During each hospitalization every procedure will be recorded and details surrounding each bleeding event related to a procedure will be recorded.

Sponsors and collaborators

Lead sponsor

University of Virginia

Other

Registry information

Acronym: PROC-BLeeD

Important dates

Study start
2019
Primary completion
2022
Study completion
2022
First posted
Sep 3, 2019
Registry last updated
Nov 4, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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