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A Multicenter Phase II Study of Neoadjuvant Docetaxel, Cisplatin and Capecitabine combined with Protocolized Surgery in Resectable Gastric Cancer - DoCCS

Conditions
Gastric carcinoma stadium Ib-IVa
MedDRA version: 9.1Level: LLTClassification code 10017770Term: Gastric carcinoma
MedDRA version: 9.1Level: LLTClassification code 10008452Term: Chemotherapy multiple agents systemic
Registration Number
EUCTR2007-007273-23-NL
Lead Sponsor
Jeroen Bosch Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Authorised-recruitment may be ongoing or finished
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Ib-IVa histological proven resectable gastric adenocarcinoma
WHO < or = 1
Age > or = 18 years
No prior radio- or chemotherapy

Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Ia gastric cancer
Other histological type than adenocarcinoma
Distant metastases
Inoperable patients
Other current serious illness or medical conditions
Known hypersensitivity to Docetaxel/Taxotere
Pregnant or lactating women

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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