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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03534843
Other study ID # Chenxp011
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2005
Est. completion date January 1, 2018

Study information

Verified date May 2018
Source Huazhong University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To compare Child-Pugh and Albumin-Bilirubin scores in patients with spontaneous rupture of hepatocellular carcinoma


Description:

To compare Child-Pugh and Albumin-Bilirubin scores in patients with spontaneous rupture of hepatocellular carcinoma. And to determine which is better in predicting long-term survival and short-term survival.


Recruitment information / eligibility

Status Completed
Enrollment 230
Est. completion date January 1, 2018
Est. primary completion date August 1, 2015
Accepts healthy volunteers No
Gender All
Age group 15 Years to 76 Years
Eligibility Inclusion Criteria:

- Be diagnosed as hepatocellular carcinoma pathologically; had a tumor rupture confirmed by Intraperitoneal exploration or clinical signs and symptoms in combination with imaging examination.

Exclusion Criteria:

- Be diagnosed as not hepatocellular carcinoma pathologically;had repeated transcatheter arterial chemoembolization(TACE) or a long history (more than 1 year) of cancer treatment; loss of follow up or without complete data.

Study Design


Intervention

Procedure:
Liver resection
Liver resection was comprised of single or multiple liver resections aiming to excise all macroscopic tumors.
Other:
Transcatheter arterial embolization
Transcatheter arterial embolization or transcatheter arterial chemoembolization can localize the bleeding point and provide interventional embolization.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Huazhong University of Science and Technology

Outcome

Type Measure Description Time frame Safety issue
Primary Overall survival of all patients Overall survival of all patients among different Child-Pugh and albumin-bilirubin scores 5 years
Secondary Short-term mortality of all patients Ninety-day mortality of all patients among different Child-Pugh and albumin-bilirubin scores Ninety days
Secondary Short-term mortality of surgical subgroup Ninety-day mortality of the surgical subgroup among different Child-Pugh and albumin-bilirubin scores Ninety days
Secondary Short-term mortality of non-surgical subgroup Ninety-day mortality of the non-surgical subgroup among different Child-Pugh and albumin-bilirubin scores Ninety days
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