NCT03281278

Brief Summary

Ineffective hemostasis or a paradoxical prothrombotic state of Acute-on-chronic liver disease (ACLF) has been well established. Thrombelastography measures the dynamics of thrombin production and provides a global assessment of coagulation incorporating the cumulative effect of the interactions at various levels between plasma components and cellular component of coagulation. And through the platelet mapping, it can help provide a picture of patients' function of platelet. This study aims to explore the predictive role of platelet mapping in ACLF prognosis, organ failure developments and short term mortality.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Oct 2017

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 11, 2017

Completed
2 days until next milestone

First Posted

Study publicly available on registry

September 13, 2017

Completed
2 months until next milestone

Study Start

First participant enrolled

October 30, 2017

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 13, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 13, 2018

Completed
Last Updated

June 6, 2019

Status Verified

April 1, 2018

Enrollment Period

10 months

First QC Date

September 11, 2017

Last Update Submit

June 4, 2019

Conditions

Keywords

Thrombelastography,acute on chronic liver failure, platelet

Outcome Measures

Primary Outcomes (1)

  • 28-day mortality

    death within 28-day

    28-day

Secondary Outcomes (2)

  • 28-day progression

    28-day

  • 90-day mortality

    90-day

Interventions

standard medical treatment

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with HBV-related chronic liver disease, International Normalized Ratio (INR)≥1.5 and total bilirubin≥85μmol/L

You may qualify if:

  • patient with previously diagnosed or undiagnosed HBV related chronic liver disease/cirrhosis
  • INR≥1.5 and total bilirubin≥85μmol/L

You may not qualify if:

  • INR≤1.5 or total bilirubin≤85μmol/L;
  • underlying chronic liver disease was other than chronic HBV infection related;
  • those who had hepatocellular carcinoma or other types of malignancies;
  • obstructive biliary diseases or other disease lead to bilirubin evaluation;
  • those who had acute hemorrhage one week before admission
  • those who received platelet, cryo transfusion or plasmapheresis one week before admission
  • using steroid or immunosuppressant or antiplatelet or anticoagulant drugs in 4 weeks
  • any kind of decompensation which persisted over a month
  • pregnancy and breastfeeding
  • those who received liver transplantation or kidney transplantation;
  • combine with other disease lead to organ failure including heart failure (NYHA IV),respiratory failure(PaO2\<60mmHg),renal insufficiency(CKD 5) and conscious disturbance (GCS\<8)
  • readmission;
  • death within 24 hours.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Nanfang Hospital

Guangzhou, Guangdong, 510515, China

Location

MeSH Terms

Conditions

Acute-On-Chronic Liver Failure

Condition Hierarchy (Ancestors)

Liver Failure, AcuteLiver FailureHepatic InsufficiencyLiver DiseasesDigestive System Diseases

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 11, 2017

First Posted

September 13, 2017

Study Start

October 30, 2017

Primary Completion

August 13, 2018

Study Completion

August 13, 2018

Last Updated

June 6, 2019

Record last verified: 2018-04

Locations