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Completed Phase 2 Interventional Results available

Intensity-Modulated Radiation Therapy, Cisplatin, and Bevacizumab Followed by Carboplatin and Paclitaxel in Treating Patients Who Have Undergone Surgery for Endometrial Cancer

ClinicalTrials.gov ID: NCT01005329

Public ClinicalTrials.gov record NCT01005329. 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 Sep 4, 2026, 8:41 PM 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 II Study of Postoperative Intensity Modulated Radiation Therapy (IMRT) With Concurrent Cisplatin and Bevacizumab Followed by Carboplatin and Paclitaxel for Patients With Endometrial Cancer

Brief summary

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

This phase II trial studies the side effects of giving intensity-modulated radiation therapy together with cisplatin and bevacizumab followed by carboplatin and cisplatin and to see how well they work in treating patients who have undergone surgery for high-risk endometrial cancer. Specialized radiation therapy that delivers a high dose of radiation directly to the tumor may kill more tumor cells and cause less damage to normal tissue. Drugs used in chemotherapy, such as cisplatin, carboplatin, and paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as bevacizumab, can block the ability of tumor cells to grow and spread. Bevacizumab may also stop the growth of tumor cells by blocking blood flow to the tumor. Giving intensity-modulated radiation therapy together with chemotherapy and bevacizumab after surgery may kill any tumor cells that remain after surgery.

Study identification

NCT ID
NCT01005329
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
34 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
Nov 5, 2009
Primary completion
Jun 29, 2012
Completion
Sep 21, 2013
Last update posted
Mar 14, 2018

2009 – 2013

United States locations

U.S. sites
38
U.S. states
20
U.S. cities
34
Facility City State ZIP Site status
Alta Bates Summit Medical Center-Herrick Campus Berkeley California 94704
John Muir Medical Center-Walnut Creek Walnut Creek California 94598
Penrose-Saint Francis Healthcare Colorado Springs Colorado 80907
Poudre Valley Hospital Fort Collins Colorado 80524
Christiana Care Health System-Christiana Hospital Newark Delaware 19718
Baptist MD Anderson Cancer Center Jacksonville Florida 32207
Integrated Community Oncology Network-Southside Cancer Center Jacksonville Florida 32207
University of Florida Health Science Center - Jacksonville Jacksonville Florida 32209
Baptist Medical Center South Jacksonville Florida 32258
Integrated Community Oncology Network-Florida Cancer Center Beaches Jacksonville Beach Florida 32250
21st Century Oncology-Orange Park Orange Park Florida 32073
21st Century Oncology-Palatka Palatka Florida 32177
Bay Medical Center Panama City Florida 32401
Integrated Community Oncology Network-Flager Cancer Center Saint Augustine Florida 32086
Northwestern University Chicago Illinois 60611
John H Stroger Jr Hospital of Cook County Chicago Illinois 60612
Saint Vincent Anderson Regional Hospital/Cancer Center Anderson Indiana 46016
Saint Vincent Hospital and Health Care Center Indianapolis Indiana 46260
Kansas City NCI Community Oncology Research Program Prairie Village Kansas 66208
University of Maryland/Greenebaum Cancer Center Baltimore Maryland 21201
Central Maryland Radiation Oncology in Howard County Columbia Maryland 21044
Brigham and Women's Hospital Boston Massachusetts 02115
Henry Ford Hospital Detroit Michigan 48202
West Michigan Cancer Center Kalamazoo Michigan 49007
Elliot Hospital Manchester New Hampshire 03103
Stony Brook University Medical Center Stony Brook New York 11794
Wake Forest University Health Sciences Winston-Salem North Carolina 27157
Summa Akron City Hospital/Cooper Cancer Center Akron Ohio 44304
Summa Barberton Hospital Barberton Ohio 44203
Flower Hospital Sylvania Ohio 43560
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104
Paoli Memorial Hospital Paoli Pennsylvania 19301
Radiation Therapy Oncology Group Philadelphia Pennsylvania 19103
Lankenau Medical Center Wynnewood Pennsylvania 19096
M D Anderson Cancer Center Houston Texas 77030
Huntsman Cancer Institute/University of Utah Salt Lake City Utah 84112
Wheeling Hospital/Schiffler Cancer Center Wheeling West Virginia 26003
Froedtert and the Medical College of Wisconsin Milwaukee Wisconsin 53226

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 3 non-U.S. sites.

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About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01005329, 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 Mar 14, 2018 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01005329 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →