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Trials / Completed

CompletedNCT02259647

Sorafenib Plus Vitamin K1 Versus Sorafenib in Advanced Hepatocellular Carcinoma

Sorafenib Plus Vitamin K1 Versus Sorafenib in Advanced Hepatocellular Carcinoma - a Randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Institute of Liver and Biliary Sciences, India · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

60 patients of radiological, biopsy proven advanced HCC (Hepatocellular carcinoma) patient will be randomized into two groups. Cases group will receive Sorafenib plus vitamin K and control group will receive Sorafenib plus placebo

Conditions

Interventions

TypeNameDescription
DRUGSorafenib 400mg twice daily + intravenous infusion ofVit K1Sorafenib 400mg twice daily + intravenous infusion ofVit K1 50 mg/day with daily increase of dose by 50 mg for 6 days, followed by oral Vitamin K1 20mg twice daily for 3month
DRUGSorafenib 400 mg twice daily + Intravenousinfusion of placeboSorafenib 400 mg twice daily + Intravenousinfusion ofplacebo daily for 6 days, followed by oral placebo twice daily x 3month

Timeline

Start date
2014-10-01
Primary completion
2015-10-31
Completion
2015-10-31
First posted
2014-10-08
Last updated
2019-10-28

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT02259647. Inclusion in this directory is not an endorsement.

Sorafenib Plus Vitamin K1 Versus Sorafenib in Advanced Hepatocellular Carcinoma (NCT02259647) · Clinical Trials Directory