Type of Study:

Interventional

Study Design:

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Safety of intraperitoneal FUDR

Outcome Description:

This protocol is testing the safety of giving two cycles of intraperitoneal FUDR followed by the conventional postoperative chemo-radiation for gastric cancer

Outcome Time Frame:

three months after surgery

Safety Issue:

Yes

Authority:

United States: Food and Drug Administration

Study ID:

2150

NCT ID:

NCT00058916

Start Date:

September 2002

Completion Date:

December 2009

Related Keywords:

• Stomach Neoplasms
• Neoplasms
• Carcinoma
• Stomach Neoplasms

Name	Location
New York University School of Medicine	New York, New York  10016
University of Southern California	Los Angeles, California  90033