A Comparison Between Child-Pugh and Albumin-Bilirubin Scores
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|ClinicalTrials.gov Identifier: NCT03534843|
Recruitment Status : Completed
First Posted : May 23, 2018
Last Update Posted : May 28, 2018
|Condition or disease||Intervention/treatment|
|Rupture, Spontaneous Rupture Liver Hepatocellular Carcinoma Hepatic Impairment||Procedure: Liver resection Other: Transcatheter arterial embolization|
|Study Type :||Observational|
|Actual Enrollment :||230 participants|
|Official Title:||A Comparison Between Child-Pugh and Albumin-Bilirubin Scores in Patients With Spontaneous Rupture of Hepatocellular Carcinoma: A Retrospective Study|
|Actual Study Start Date :||January 1, 2005|
|Actual Primary Completion Date :||August 1, 2015|
|Actual Study Completion Date :||January 1, 2018|
Patients who received liver resection or palliative surgery, such as microwave coagulation therapy, hepatic artery ligation, or suturing ligation.
Procedure: Liver resection
Liver resection was comprised of single or multiple liver resections aiming to excise all macroscopic tumors.
Patients who received transcatheter arterial embolization (or transcatheter arterial chemoembolization) or conservative treatment
Other: Transcatheter arterial embolization
Transcatheter arterial embolization or transcatheter arterial chemoembolization can localize the bleeding point and provide interventional embolization.
- Overall survival of all patients [ Time Frame: 5 years ]Overall survival of all patients among different Child-Pugh and albumin-bilirubin scores
- Short-term mortality of all patients [ Time Frame: Ninety days ]Ninety-day mortality of all patients among different Child-Pugh and albumin-bilirubin scores
- Short-term mortality of surgical subgroup [ Time Frame: Ninety days ]Ninety-day mortality of the surgical subgroup among different Child-Pugh and albumin-bilirubin scores
- Short-term mortality of non-surgical subgroup [ Time Frame: Ninety days ]Ninety-day mortality of the non-surgical subgroup among different Child-Pugh and albumin-bilirubin scores
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03534843
|Study Chair:||Xiao-ping Chen, Prof. PHD||Huazhong University of Science and Technology|