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Uterine Cervical Neoplasms clinical trials

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NCT ID: NCT00276796 Completed - Cervical Cancer Clinical Trials

Paclitaxel, Topotecan, and Cisplatin in Treating Patients With Advanced, Persistent, or Recurrent Cervical Cancer

Start date: n/a
Phase: Phase 2
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as paclitaxel, topotecan, 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) may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving paclitaxel together with topotecan and cisplatin works in treating patients with advanced, persistent, or recurrent cervical cancer.

NCT ID: NCT00275353 Completed - Cervical Cancer Clinical Trials

Effectiveness of an Individualized Symptom Education Program (ISEP)

Start date: July 2003
Phase: Phase 2
Study type: Interventional

The purpose of this study is to examine whether an Individualized Symptom Education Program (ISEP) is helpful to women to manage their symptoms when they are receiving radiation therapy for gynecological cancer. It is expected that women who participate in the ISEP program will be better able to manage their symptoms and exprience less distress than women who receive usual care.

NCT ID: NCT00268918 Completed - Breast Cancer Clinical Trials

Docetaxel and PTK787 in Metastatic Breast Cancer Patients and Gynecological Cancer Patients

Start date: September 2005
Phase: Phase 1
Study type: Interventional

The main purpose of this study is to see if the study drug, PTK787, is safe and to find the highest dose that can be given safely without causing serious side effects.

NCT ID: NCT00266084 Completed - Clinical trials for Uterine Cervical Cancer

Clinical Trial for the Use of a Novel Cell Collector Device to Retrieve Cells From the Uterine Cervix

Start date: August 1999
Phase: Phase 1/Phase 2
Study type: Observational

This study tested the safety and performance of a new cell collector device and compared the results to those obtained with the current existing device that are being used routinely

NCT ID: NCT00260039 Completed - Cervical Cancer Clinical Trials

Broad Spectrum HPV Vaccine Dose Ranging Study (V502-001)

Start date: December 2005
Phase: Phase 2
Study type: Interventional

This dose-ranging study is to evaluate an investigational vaccine with the following objectives: (1) To demonstrate that the vaccine is well-tolerated in women (2) To evaluate immune responses in women who are between 16 and 23 years of age at enrollment.

NCT ID: NCT00258401 Completed - Prostate Cancer Clinical Trials

Low-Residue Diet in Treating Diarrhea in Patients Receiving Pelvic Radiation Therapy.

Start date: May 2005
Phase: N/A
Study type: Interventional

RATIONALE: Eating a diet low in residue (fiber, fat, and certain milk or vegetable products) may help prevent or reduce diarrhea caused by pelvic radiation therapy. PURPOSE: This randomized clinical trial is studying a low-residue diet to see how well it works compared to no dietary intervention in treating diarrhea in patients who are undergoing radiation therapy to the pelvis for uterine, cervical, or prostate cancer.

NCT ID: NCT00257816 Completed - Cervical Cancer Clinical Trials

Weekly IV Topotecan and Cisplatin With Radiation in Cervical Carcinoma

Start date: January 2004
Phase: Phase 2
Study type: Interventional

There will be approximately 14,000 new patients with invasive cervical cancer diagnosed in the United States in 2003 with about 4,000 deaths from this disease. This accounts for approximately 17% of all deaths due to gynecologic cancers. Radiation has been the primary treatment modality for locoregionally advanced cervical cancer. Recent trials of concomitant systemic cisplatin chemotherapy and radiation have shown high response rates (RR) with improvements in durable remissions and overall survival. Though the incidence and mortality in the U.S. dropped steadily from years 1940 to 2000, there has recently been a plateau, arresting the decline. With the routine addition of systemic Cisplatin (CDDP) chemotherapy to local regional radiation, mortality from advanced cervical cancer in the United States is expected to further decrease. However, further advances in this disease are needed.

NCT ID: NCT00257348 Completed - Cervical Cancer Clinical Trials

Capecitabine and Docetaxel in Advanced/Recurrent Cervical Cancer

Start date: March 2004
Phase: Phase 2
Study type: Interventional

The purpose of the study is to evaluate the effectiveness and side effects of the drugs capecitabine and docetaxel in the treatment of cervical cancer. Capecitabine is approved by the FDA for the treatment of breast and colon cancer. Docetaxel is approved in the treatment of breast and lung cancer. The use of capecitabine and docetaxel in this study for the treatment of cervical cancer is considered investigational. Eligible subjects will take the drug capecitabine (Xeloda) by mouth twice a day every 12 hours, for fourteen consecutive days followed by a 7 day rest period. Subjects will also receive the drug docetaxel (Taxotere) intravenously (in the vein) every three weeks.

NCT ID: NCT00251888 Completed - Cervix Cancer Clinical Trials

CAmpto-CISplatine Plus Radiotherapy in Advanced Cervix Cancer : Search of Tolerated Maximum Dose of Campto

Start date: November 2002
Phase: Phase 1
Study type: Interventional

Search of maximum tolerated irinotecan dose in association with cisplatin and pelvic radiotherapy in patients with an advanced cervix cancer.

NCT ID: NCT00242034 Completed - Cervix Cancer Clinical Trials

Investigation of Cervix Tumor Oxygenation and Microvasculature Using Magnetic Resonance Techniques

Start date: n/a
Phase: N/A
Study type: Interventional

In cervix cancer tumor oxygen levels and fluid pressure in the tumor have been shown to be related to patient outcome. Analysis of the way tumors enhance after intravenous contrast injection using MRI and CT can be used to determine parameters that relate to tumor blood vessels. In this study we hope to determine if there is a relationship between the enhancement of cervix cancer on MRI and CT and tumor oxygen levels and interstitial fluid pressure. If such a relationship exists then it could help improve the care of patients wiht cervix cancer by allowing for more aggressive therapy of patients with cancer that have more ominous imaging characteristics