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Completed Phase 1Phase 2 Interventional

Radiation Therapy Plus Celecoxib, Fluorouracil, and Cisplatin in Patients With Locally Advanced Cervical Cancer

ClinicalTrials.gov ID: NCT00023660

Public ClinicalTrials.gov record NCT00023660. 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 Nov 10, 2026, 12:38 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase I/II Study Of COX-2 Inhibitor, CELEBREX (CELECOXIB), And Chemoradiation In Patients With Locally Advanced Cervical Cancer

Brief summary

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

RATIONALE: Radiation therapy uses high-energy x-rays to damage tumor cells. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Giving radiation therapy in different ways and combining it with chemotherapy may kill more tumor cells. Celecoxib may slow the growth of cervical cancer by stopping blood flow to the tumor. PURPOSE: Phase I/II trial to study the effectiveness of radiation therapy plus celecoxib, fluorouracil, and cisplatin in treating patients who have locally advanced cervical cancer.

Study identification

NCT ID
NCT00023660
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Enrollment
84 participants

Conditions and interventions

Interventions

Drug · Radiation

Eligibility (public fields only)

Age range
18 Years to 85 Years
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
Aug 2001 (Type not available)
Primary completion
Jan 2005 (Actual)
Completion
Not listed
Last update posted
Nov 19, 2013

Started 2001

United States locations

U.S. sites
36
U.S. states
20
U.S. cities
33
Facility City State ZIP Site status
Mobile Infirmary Medical Center Mobile Alabama 36652-2144 —
Foundation for Cancer Research and Education Phoenix Arizona 85013 —
Mills-Peninsula Health Services Burlingame California 94010 —
Sutter Health Western Division Cancer Research Group Greenbrae California 94904 —
UCSF Comprehensive Cancer Center San Francisco California 94143-0128 —
Memorial Hospital Cancer Center Colorado Springs Colorado 80909 —
Baptist Hospital of Miami Miami Florida 33256-2110 —
Regional Radiation Oncology Center at Rome Rome Georgia 30165 —
Methodist Medical Center of Illinois Peoria Illinois 61636 —
Ball Memorial Hospital Cancer Center Muncie Indiana 47303-3499 —
West Michigan Cancer Center Kalamazoo Michigan 49007 —
CCOP - Kansas City Kansas City Missouri 64131 —
Methodist Hospital Cancer Center at Nebraska Methodist Hospital - Omaha Omaha Nebraska 68114-4199 —
CCOP - Southern Nevada Cancer Research Foundation Las Vegas Nevada 89106 —
Monmouth Medical Center Long Branch New Jersey 07740-6395 —
South Jersey Regional Cancer Center Millville New Jersey 08332 —
Fox Chase Virtua Health Cancer Program at Virtua Memorial Hospital Mount Holly New Jersey 08060 —
Newark Beth Israel Medical Center Newark New Jersey 07112 —
Community Medical Center Toms River New Jersey 08755 —
State University of New York Health Science Center at Brooklyn Brooklyn New York 11203 —
New York Methodist Hospital Brooklyn New York 11215 —
Comprehensive Cancer Center at Wake Forest University Winston-Salem North Carolina 27157-1065 —
Akron General Medical Center Akron Ohio 44302 —
Akron City Hospital - Summa Health System Akron Ohio 44304 —
Bryn Mawr Hospital Bryn Mawr Pennsylvania 19010 —
Mercy Fitzgerald Hospital Darby Pennsylvania 19023 —
Delaware County Memorial Hospital Drexel Hill Pennsylvania 19026 —
Paoli Memorial Hospital Paoli Pennsylvania 19301-1792 —
Kimmel Cancer Center at Thomas Jefferson University - Philadelphia Philadelphia Pennsylvania 19107-5097 —
Western Pennsylvania Hospital Pittsburgh Pennsylvania 15224 —
CCOP - MainLine Health Wynnewood Pennsylvania 19096 —
Lankenau Cancer Center at Lankenau Hospital Wynnewood Pennsylvania 19096 —
University of Texas - MD Anderson Cancer Center Houston Texas 77030-4009 —
LDS Hospital Salt Lake City Utah 84143 —
Dixie Regional Medical Center St. George Utah 84770 —
CCOP - Marshfield Clinic Research Foundation Marshfield Wisconsin 54449 —

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 NCT00023660, 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 Nov 19, 2013 · Synced Nov 10, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00023660 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →