Clinical Trials Directory

Trials / Completed

CompletedNCT02991339

The Effects of Dexamethasone Administration on Jaundice Following Liver Resection

The Effects of Dexamethasone Administration on Jaundice Following Liver Resection: a Randomized Controlled Trial

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
76 (actual)
Sponsor
Shanghai Zhongshan Hospital · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The investigators were aiming to evaluate whether dexamethasone administration accelerates the recovery from hepatectomy-related jaundice and decreases the rates of post-hepatectomy liver failure and its safety in the subjects who developed elevated serum total bilirubin.

Detailed description

Post-operative jaundice is one of the most common complications after hepatectomy for various liver tumors. Glucocorticoids, including dexamethasone, prednisolone, and methylprednisolone, were widely used to treat jaundice in the patients with severe hepatitis, liver dysfunction or liver failure. It was reported that glucocorticoids decrease the rates of liver dysfunction or mortality in those patients. However, whether post-operative glucocorticoids administration alleviated jaundice or deceased the rates of post-hepatectomy liver failure (PLF) yet to be determined. In this study, the investigators were aiming to evaluate whether dexamethasone administration accelerates the recovery from hepatectomy-related jaundice and decreases the rates of PLF and its safety in the subjects who developed elevated serum TB.

Conditions

Interventions

TypeNameDescription
DRUGDexamethasoneDexamethasone 10 mg iv for 2 days; then 5 mg iv for 1 day

Timeline

Start date
2016-06-01
Primary completion
2017-12-01
Completion
2018-07-01
First posted
2016-12-13
Last updated
2021-06-10

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02991339. Inclusion in this directory is not an endorsement.