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Clinical Trial Details — Status: Suspended

Administrative data

NCT number NCT01608945
Other study ID # EHBH112
Secondary ID
Status Suspended
Phase N/A
First received May 29, 2012
Last updated May 30, 2012
Start date April 2008

Study information

Verified date May 2012
Source Eastern Hepatobiliary Surgery Hospital
Contact n/a
Is FDA regulated No
Health authority China: Ethics Committee
Study type Observational

Clinical Trial Summary

The major drawback of hepatic pedicle clamping is ischaemia-reperfusion injury with impairment of liver function. Perioperative steroid administration has been advocated to reduce liver damage. The aim of this prospective, randomized study was to determine whether steroid administration can reduce liver injury and impact the prognosis


Recruitment information / eligibility

Status Suspended
Enrollment 60
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- 18-70 years old

- diametre of the mass>3cm.

- hcc

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Some Studies Shows That the Steroid Can Reduce the Injury of the I/R of the Liver

Intervention

Drug:
Hydrocortisone sodium succinate
100mg/day

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Eastern Hepatobiliary Surgery Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary liver function six months No