Clinical Trials Directory

Trials / Unknown

UnknownNCT01558947

Peri-operative Chemotherapy With ECX or XP in the Treatment of Advanced Gastric Cancer

Peri-operative Chemotherapy With ECX (Epirubicin + Cisplatin + Capecitabine) or XP (Capecitabine + Cisplatin) in the Treatment of Advanced Gastric Cancer: a Randomized, Multicenter, Parallel Control

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
2 (estimated)
Sponsor
Zhejiang Cancer Hospital · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the safety and the effect of perioperative chemotherapy in the treatment of advanced gastric cancer.

Detailed description

To evaluate the security and the relapse-free survival time/rate(1,2,3 yrs) of perioperative chemotherapy with ECX (epirubicin + cisplatin + capecitabine) and XP (capecitabine + cisplatin)in advanced gastric cancer

Conditions

Interventions

TypeNameDescription
DRUGPeri-operative chemotherapy of ECXPreoperative chemotherapy of ECX for 3 cycles(Epirubicin 50mg/m2 on day 1; capecitabine 1000mg/m2, 2 times / day, 1 to 14 days; cisplatin 60mg/m2 on day 1, need hydration, 21 day/cycle), operation after 2\~4 weeks, and postoperative chemotherapy of ECX for 3 cycles 4\~6 weeks after surgery.
DRUGPeri-operative chemotherapy of XPPreoperative chemotherapy of XP for 3 cycles(capecitabine 1000mg/m2, 2 times / day, 1 to 14 days; cisplatin 60mg/m2 on day 1, need hydration, 21 day/cycle), operation after 2\~4 weeks, and postoperative chemotherapy of XP for 3 cycles 4\~6 weeks after surgery.

Timeline

Start date
2011-01-01
Primary completion
2012-12-01
Completion
2013-06-01
First posted
2012-03-20
Last updated
2012-03-20

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT01558947. Inclusion in this directory is not an endorsement.