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Clinical Trial Summary

There has been no report on whether the patients with gastric cancer who are also inactive Hepatitis B carriers should receive prophylactic use or preemptive Use of an Anti-viral Drug Entecavir. This open, randomized controlled clinical trial aims to compare the impact of the prophylactic use or preemptive use of an anti-viral drug Entecavir on the outcomes of patients with gastric cancer who are also inactive hepatitis B carriers during chemotherapy and the subsequent follow-ups.


Clinical Trial Description

Patients with gastric cancer who are also inactive hepatitis B carriers are enrolled and randomized into two groups as following. Patients in experimental group are treated with entecavir prophylactically in the dose of 0.5mg p.o. every day from the initiation of chemotherapy till 6 months after the end of chemotherapy.Patients in active comparator group are only treated with entecavir in the dose of 0.5mg p.o. every day from the time that the DNA copies of hepatitis B virus are more than 100 IU/ml till 6 months after the end of chemotherapy. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02777801
Study type Interventional
Source Sun Yat-sen University
Contact Rui-hua Xu, PHD,MD
Phone +86 13922206676
Email xurh@sysucc.org.cn
Status Recruiting
Phase Phase 2
Start date June 2015
Completion date June 2018

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