Evaluation of Cardiac Function in Acutely Decompensated Cirrhosis

NCT ID: NCT05413083

Last Updated: 2024-06-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Total Enrollment

70 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-06-06

Study Completion Date

2024-10-31

Brief Summary

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This project aims to investigate cardiac function in patients with cirrhosis in the acute setting. Acute decompensation and acute-on-chronic liver failure are major events in the life of a patient as they herald disease progression and negative prognosis. Cardiocirculatory function will be assessed by serial assessments in patients admitted for acute decompensation of cirrhosis.

Detailed Description

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In this project we aim to investigate the dynamic role of cardiac function in the short-term evolution of patients with AD of cirrhosis through noninvasive and accessible tests and validate prognostic imaging and serum biomarkers. The main objectives are:

1. To describe changes and evolution of cardiac function in AD of cirrhosis
2. To investigate associations between echocardiographic parameters and serum biomarkers
3. To investigate the association between ACLF and cardiac dysfunction
4. To assess the short-term prognostic impact of cardiac function in AD and ACLF;
5. To evaluate the added predictive value of cardiac markers to current scores (CLIF-C).

Conditions

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Cirrhosis Acute Liver Failure Cardiomyopathies

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* proven cirrhosis with acute decompensation

Exclusion Criteria

* screening after \> 72 hours from admission
* previous severe cardiac conditions (e.g. ischemic heart disease, atrial fibrillation, congestive heart failure, ICD)
* concomitant severe disease (e.g. active neoplasia, severe COPD, etc)
* lack of informed consent
* intubated/ comatose patient
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Clinical Hospital Colentina

OTHER

Sponsor Role lead

Responsible Party

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Andrei Voiosu

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Spitalul clinic Colentina

Bucharest, , Romania

Site Status

Countries

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Romania

Other Identifiers

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DYNACORD-AD

Identifier Type: -

Identifier Source: org_study_id

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