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Completed Phase 1 Interventional

Intraperitoneal Paclitaxel, Doxorubicin Hydrochloride, and Cisplatin in Treating Patients With Stage III-IV Endometrial Cancer

ClinicalTrials.gov ID: NCT00575952

Public ClinicalTrials.gov record NCT00575952. 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 29, 2026, 11:21 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 Phase I Study of IV Doxorubicin Plus Intraperitoneal (IP) Paclitaxel and IV or IP Cisplatin in Endometrial Cancer Patients at High Risk for Peritoneal Failure

Brief summary

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

This phase I trial studies the side effects and best dose of intraperitoneal paclitaxel when given together with doxorubicin hydrochloride and cisplatin in treating patients with stage III-IV endometrial cancer. Drugs used in chemotherapy, such as paclitaxel, doxorubicin hydrochloride, and cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) and giving them in different ways may kill more tumor cells.

Study identification

NCT ID
NCT00575952
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Gynecologic Oncology Group
Network
Enrollment
27 participants

Conditions and interventions

Eligibility (public fields only)

Age range
Not listed
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
Jan 17, 2008 (Actual)
Primary completion
Jul 16, 2016 (Actual)
Completion
Jul 16, 2016 (Actual)
Last update posted
Aug 24, 2017

2008 – 2016

United States locations

U.S. sites
9
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
Hartford Hospital Hartford Connecticut 06102 —
The Hospital of Central Connecticut New Britain Connecticut 06050 —
University of Chicago Comprehensive Cancer Center Chicago Illinois 60637 —
University of Iowa/Holden Comprehensive Cancer Center Iowa City Iowa 52242 —
Washington University School of Medicine St Louis Missouri 63110 —
Cooper Hospital University Medical Center Camden New Jersey 08103 —
Case Western Reserve University Cleveland Ohio 44106 —
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104 —
Women and Infants Hospital Providence Rhode Island 02905 —

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 NCT00575952, 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 Aug 24, 2017 · Synced Oct 29, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00575952 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →