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Cervical Cancer clinical trials

View clinical trials related to Cervical Cancer.

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NCT ID: NCT00381888 Completed - Ovarian Cancer Clinical Trials

Fondaparinux in Preventing Blood Clots in Patients Undergoing Surgery for Gynecologic Cancer

Start date: January 2007
Phase: Phase 2
Study type: Interventional

RATIONALE: Fondaparinux may help prevent blood clots from forming in patients who are undergoing surgery for gynecologic cancer. PURPOSE: This phase II trial is studying how well fondaparinux works in preventing blood clots in patients undergoing surgery for gynecologic cancer.

NCT ID: NCT00380055 Completed - Breast Cancer Clinical Trials

Reducing Cancer Disparities for American Indians in the Rural Intermountain West

Start date: October 2006
Phase: N/A
Study type: Interventional

The purpose of this demonstration is to evaluate the effectiveness of using community outreach workers (navigators) to help American Indians living in rural areas overcome barriers to appropriate cancer screening, diagnosis, and treatment.

NCT ID: NCT00379782 Completed - Breast Cancer Clinical Trials

Kukui Ahi Navigator Cancer Screening and Treatment Demonstration Project

Start date: October 2006
Phase: N/A
Study type: Interventional

This Cancer Prevention and Treatment Demonstration Project funded by the Centers of Medicare and Medicaid Services awarded six sites across the United States to develop Patient Navigator Programs to eliminate disparities in the rate of preventative cancer screening and timely diagnosis and treatment of cancer for racial and ethnic minorities. This site of Molokai General Hospital are focused on Pacific Islanders and Asian Americans. This program called Kukui Ahi propose to increase screening and early detection for four targeted cancers-breast, cervical, colorectal, and prostate- with lung cancer additionally being included in treatment protocols to improve outcomes and satisfaction by employing a culturally appropriate navigation protocol to facilitate utilization of healthcare services and decrease health barriers. The specific aims of the project is to: 1. Determine if a Navigator Program can reduce the proportion of the targeted cancers diagnosed at a late stage, 2. Determine if the Navigator Program can improve the continuity of health care for cancer patients, 3. Determine if the Navigator Program can improve quality of life and subjective well being of navigated cancer patients, 4. Determine if the Navigator Program is a cost-effective way to reduce cancer care disparities for screenable cancers.

NCT ID: NCT00376987 Completed - Lung Cancer Clinical Trials

Zinc Supplements in Lowering Cadmium Levels in Smokers

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

RATIONALE: Zinc supplements may lower cadmium levels in smokers and may help prevent DNA damage. PURPOSE: This clinical trial is studying how well zinc supplements work in lowering cadmium levels in smokers.

NCT ID: NCT00376909 Completed - Breast Cancer Clinical Trials

A Telephone-Based Prevention Care Manager in Increasing Screening Rates for Breast Cancer, Cervical Cancer, and Colorectal Cancer in Minority and Low-Income Women

Start date: November 2001
Phase: Phase 2
Study type: Interventional

RATIONALE: Studying the barriers that prevent minority and low-income women from undergoing cancer screening, and offering encouragement to them over the telephone, may help improve cancer screening rates. PURPOSE: This randomized phase II trial is studying how well a telephone-based Prevention Care Manager increases screening rates for breast cancer, cervical cancer, and colorectal cancer in minority and low-income women.

NCT ID: NCT00365508 Completed - Lung Cancer Clinical Trials

Counseling and Nicotine Replacement Therapy in Helping Adult Smokers Quit Smoking

Start date: February 2006
Phase: Phase 4
Study type: Interventional

RATIONALE: Stop-smoking plans, including counseling and nicotine replacement therapy, may help smokers quit smoking. It is not yet known whether counseling and the nicotine lozenge is more effective than counseling and the nicotine patch in helping adult smokers quit smoking. PURPOSE: This randomized phase III trial is studying counseling and the nicotine lozenge to see how well they work compared to counseling and the nicotine patch in helping smokers quit smoking.

NCT ID: NCT00340184 Completed - Cervical Cancer Clinical Trials

A Safety and Efficacy of CCRT With Paclitaxel/Carboplatin as Adjuvant Therapy to Post-operative Cervical Cancer Patients

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

The purpose of this study is to determine whether post-operative concurrent chemoradiation with paclitaxel/carboplatin is effective and safe in the treatment of high risk cervical cancer patients.

NCT ID: NCT00339989 Completed - Cervical Cancer Clinical Trials

Cervical Cancer Early Endpoints and Determinants

Start date: September 12, 2003
Phase:
Study type: Observational

This study, conducted by the National Cancer Institute and the University of Oklahoma, will look for changes in cervix cells and other samples that may be signs of cervical disease. Human papilloma virus, or HPV, is a common infection of the genitalia in women that usually goes away by itself. If HPV infection does not go away, it might turn into cancer of the cervix, although this is rare. This study will examine why many HPV infections go away and why a few persist and lead to cervical cancer. Women 18 years of age and older who are referred for colposcopy (examination of the vagina and cervix using an instrument with a magnifying lens) at the University of Oklahoma following Pap smear diagnosis may be eligible for this study. Women will be in one of the following diagnostic categories: - Cancer: Stage 1-2 only. - Precancer: Cervical intraepithelial neoplasia (CIN3). - HPV-infected: Positive for any of the 13 known cancer-causing HPV types, but not diagnosed with cancer or CIN3. - Normal: Negative for cancer-causing HPV and normal tissue laboratory results. Participants will undergo the following procedures: - Questionnaire: Covers demographic information (such as age, race, ethnicity, marital status, etc.), pregnancy history, menstrual and sexual history, contraceptive history, hormone medication history, medical history, smoking history, physical development, family history, and health care access. - Blood test: 2 tablespoons of blood drawn. - Colposcopy. - Procedure to collect a sample of cervical cells and fluids for HPV testing and research.

NCT ID: NCT00331760 Completed - Cervical Cancer Clinical Trials

Intensity-Modulated Radiation Therapy to the Pelvis With or Without Chemotherapy in Treating Patients With Endometrial Cancer or Cervical Cancer That Has Been Removed By Surgery

Start date: March 2006
Phase: Phase 2
Study type: Interventional

RATIONALE: Specialized radiation therapy (RT), such as intensity-modulated radiation therapy (IMRT), 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, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving intensity-modulated radiation therapy to the pelvis with or without chemotherapy after surgery may kill any tumor cells that remain after surgery. PURPOSE: This phase II trial is studying how well intensity-modulated radiation therapy to the pelvis with or without chemotherapy works in treating patients with endometrial cancer or cervical cancer that has been removed by surgery.

NCT ID: NCT00320983 Completed - Cervical Cancer Clinical Trials

Study of Adjuvant Topotecan and Cisplatin With Concurrent Radiation Therapy for Advanced Cervical Cancer

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

A Phase I Study of Adjuvant Topotecan and Cisplatin with Concurrent Radiation Therapy for Advanced Cervical Cancer.