Primary Peritoneal Carcinoma Clinical Trial
Official title:
Phase II Evaluation of Weekly Docetaxel in Combination With Weekly Carboplatin in the Treatment of Recurrent Epithelial Ovarian Carcinoma
Verified date | June 2008 |
Source | University of Wisconsin, Madison |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to determine the safety and efficacy of this regimen in women with ovarian or peritoneal cancer
Status | Completed |
Enrollment | 36 |
Est. completion date | February 2006 |
Est. primary completion date | |
Accepts healthy volunteers | |
Gender | Female |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Recurrent ovarian or peritoneal cancer Exclusion Criteria: - No prior chemotherapy |
Country | Name | City | State |
---|---|---|---|
United States | University of Wisconsin Hospital and Clinics | Madison | Wisconsin |
Lead Sponsor | Collaborator |
---|---|
University of Wisconsin, Madison | Aventis Pharmaceuticals |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Safety and Efficacy | |||
Secondary | QOL |
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