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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03204591
Other study ID # NSFC81670567
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 20, 2017
Est. completion date January 18, 2019

Study information

Verified date June 2018
Source The Zhejiang Study Group for Organ Failure in Cirrhosis
Contact Yu Shi, Doctor
Phone 86-0571-87236489
Email zjushiyu@zju.edu.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Acute hepatic insults including hepatitis flare-up, active alcohol assumption and hepatotoxic drug use are common in patients with cirrhosis especially in Eastern countries.These patients are at high risk of developing acute-on-chronic liver failure (ACLF) and associated with high short-term mortality. And the natural history of these patients is frequently complicated by bacterial infections, which lead to deterioration of underlying diseases. The present study is aimed to investigate the prevalance and risk factors of bacterial infections in those patients and its impact on in-hospital/short-term mortality.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date January 18, 2019
Est. primary completion date October 18, 2018
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

1. The presence of cirrhosis confirmed by liver biopsy, endoscopy, radiological examination, or clinical evidence of prior hepatic de-compensation;

2. Flare up of acute severe liver injury within one month before enrollment. Acute severe liver injury is defined as: increase of serum bilirubin >=85mmol/L and international normalized ratio (INR)>=1.5 with a definite hepatic insult.

Exclusion Criteria:

(1)pregnancy; (2) disseminated maliganancy; (3)previously received a liver transplant; (4) HIV infection;

Study Design


Intervention

Other:
No intervention
No intervention

Locations

Country Name City State
China First Affiliated Hospital of Zhejiang University Hangzhou Zhejiang

Sponsors (2)

Lead Sponsor Collaborator
The Zhejiang Study Group for Organ Failure in Cirrhosis Ningbo No.2 Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Occurrence of bacterial infection Site,source, pathogen and severity Within 3 months from admission
Secondary 28-day Mortality Disease-associated mortality Within 28 days after enrollment
Secondary 90-day Mortality Disease-associated mortality Within 90 days after enrollment
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