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Not listed Phase 1 Interventional

Cisplatin and Radiation Therapy Followed by Paclitaxel and Carboplatin in Treating Patients With Stage IB-IVA Cervical Cancer

ClinicalTrials.gov ID: NCT01295502

Public ClinicalTrials.gov record NCT01295502. 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 20, 2026, 1:49 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 Evaluation of Extended Field Radiation Therapy With Concomitant Cisplatin Chemotherapy Followed by Paclitaxel and Carboplatin Chemotherapy in Women With Cervical Carcinoma Metastatic to the Para-aortic Lymph Nodes

Brief summary

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

This phase I trial studies the side effects and the best dose of paclitaxel and carboplatin after cisplatin and radiation therapy in treating patients with stage IB-IVA cervical cancer. Drugs used in chemotherapy, such as cisplatin, paclitaxel, and carboplatin, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving paclitaxel and carboplatin after cisplatin and radiation therapy may kill more tumor cells.

Study identification

NCT ID
NCT01295502
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Gynecologic Oncology Group
Network
Enrollment
45 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
Apr 4, 2011 (Actual)
Primary completion
Dec 2, 2019 (Estimated)
Completion
Not listed
Last update posted
Mar 12, 2019

Started 2011

United States locations

U.S. sites
14
U.S. states
8
U.S. cities
12
Facility City State ZIP Site status
UC Irvine Health/Chao Family Comprehensive Cancer Center Orange California 92868 —
Hartford Hospital Hartford Connecticut 06102 —
The Hospital of Central Connecticut New Britain Connecticut 06050 —
Augusta University Medical Center Augusta Georgia 30912 —
University of Iowa/Holden Comprehensive Cancer Center Iowa City Iowa 52242 —
Summa Akron City Hospital/Cooper Cancer Center Akron Ohio 44304 —
Case Western Reserve University Cleveland Ohio 44106 —
MetroHealth Medical Center Cleveland Ohio 44109 —
Cleveland Clinic Foundation Cleveland Ohio 44195 —
Riverside Methodist Hospital Columbus Ohio 43214 —
Hillcrest Hospital Cancer Center Mayfield Heights Ohio 44124 —
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104 —
Women and Infants Hospital Providence Rhode Island 02905 —
Virginia Commonwealth University/Massey Cancer Center Richmond Virginia 23298 —

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 NCT01295502, 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 12, 2019 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01295502 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →