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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00214058
Other study ID # CO02701
Secondary ID 2002-224A532820S
Status Completed
Phase Phase 2
First received
Last updated
Start date August 2002
Est. completion date February 2006

Study information

Verified date June 2008
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the safety and efficacy of this regimen in women with ovarian or peritoneal cancer


Recruitment information / eligibility

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

Study Design


Intervention

Drug:
Carboplatin

Docetaxel


Locations

Country Name City State
United States University of Wisconsin Hospital and Clinics Madison Wisconsin

Sponsors (2)

Lead Sponsor Collaborator
University of Wisconsin, Madison Aventis Pharmaceuticals

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Safety and Efficacy
Secondary QOL
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