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Completed Phase 2 Interventional Results available

Paclitaxel and Carboplatin With Or Without Sorafenib In The First-Line Treatment Of Patients With Ovarian Cancer

ClinicalTrials.gov ID: NCT00390611

Public ClinicalTrials.gov record NCT00390611. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 6, 2026, 9:03 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized Phase II Study of Paclitaxel/Carboplatin With or Without Sorafenib in the First-Line Treatment of Patients With Stage III/IV Epithelial Ovarian Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This trial will compare the efficacy and toxicity of standard first-line chemotherapy alone vs. standard chemotherapy plus sorafenib in patients with stage III/IV ovarian cancer following cytoreductive surgery. Patients with residual large volume disease and/or bowel involvement will be excluded, to minimize the risk of bowel perforation.

Study identification

NCT ID
NCT00390611
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
85 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 2006 (Type not available)
Primary completion
Jul 2012 (Actual)
Completion
Apr 2014 (Actual)
Last update posted
Dec 22, 2014

2006 – 2014

United States locations

U.S. sites
17
U.S. states
11
U.S. cities
16
Facility City State ZIP Site status
Northeast Arkansas Clinic Jonesboro Arkansas 72401 —
Holy Cross Hospital Fort Lauderdale Florida 33308 —
Florida Cancer Specialists Fort Myers Florida 33901 —
Gulfcoast Oncology Associates St. Petersburg Florida 33705 —
Medical College of Georgia Cancer Specialists Augusta Georgia 30912 —
Providence Medical Group Terre Haute Indiana 47802 —
Center for Cancer and Blood Disorders Bethesda Maryland 20817 —
National Capital Clinical Research Consortium Bethesda Maryland 20817 —
St. Joseph Mercy Hospital Ann Arbor Michigan 48106 —
Grand Rapids Clinical Oncology Program Grand Rapids Michigan 49503 —
Oncology Hematology Care Cincinnati Ohio 45242 —
University of Oklahoma Oklahoma City Oklahoma 73104 —
South Carolina Oncology Associates, PA Columbia South Carolina 29210 —
Tennessee Valley Clinical Research Chattanooga Tennessee 37411 —
Family Cancer Center Collierville Tennessee 38017 —
Tennessee Oncology, PLLC Nashville Tennessee 37023 —
Peninsula Cancer Center Newport News Virginia 23601 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00390611, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 22, 2014 · Synced Oct 6, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00390611 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →