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Completed Phase 1 Interventional

Paclitaxel, Bevacizumab And Adjuvant Intraperitoneal Carboplatin in Treating Patients Who Had Initial Debulking Surgery for Stage II, Stage III, or Stage IV Ovarian Epithelial, Primary Peritoneal, or Fallopian Tube Cancer

ClinicalTrials.gov ID: NCT00079430

Public ClinicalTrials.gov record NCT00079430. 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 Jul 21, 2026, 6:58 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 Dose-Escalating Phase I Study With an Expanded Cohort to Assess the Feasibility of Intraperitoneal Carboplatin (NSC #214240) and Intravenous Paclitaxel (NSC # 673089) and Intravenous Paclitaxel, Intraperitoneal Carboplatin and NCI Supplied Intravenous Bevacizumab (NSC #704865) in Patients With Previously Untreated Epithelial Ovarian, Primary Peritoneal, or Fallopian Tube Carcinoma

Study identification

NCT ID
NCT00079430
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
National Cancer Institute (NCI)
NIH
Enrollment
113 participants

Conditions and interventions

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
May 31, 2004
Primary completion
Apr 30, 2011
Completion
Not listed
Last update posted
Jul 21, 2019

Started 2004

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
12
Facility City State ZIP Site status
University of California Medical Center At Irvine-Orange Campus Orange California 92868
University of Chicago Chicago Illinois 60637
University of Iowa Hospitals and Clinics Iowa City Iowa 52242
Johns Hopkins University/Sidney Kimmel Cancer Center Baltimore Maryland 21287
Cooper Hospital University Medical Center Camden New Jersey 08103
Wake Forest University Health Sciences Winston-Salem North Carolina 27157
Riverside Methodist Hospital Columbus Ohio 43214
Cancer Care Associates-Midtown Tulsa Oklahoma 74104
Tulsa Cancer Institute Tulsa Oklahoma 74146
Gynecologic Oncology Group Philadelphia Pennsylvania 19103
Fox Chase Cancer Center Philadelphia Pennsylvania 19111
Women and Infants Hospital Providence Rhode Island 02905
M D Anderson Cancer Center Houston Texas 77030
Pacific Gynecology Specialists Seattle Washington 98104
Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium Seattle Washington 98109
Seattle Cancer Care Alliance Seattle Washington 98109
University of Washington Medical Center Seattle Washington 98195

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00079430, 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 Jul 21, 2019 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00079430 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →