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Uterine Cervical Neoplasms clinical trials

View clinical trials related to Uterine Cervical Neoplasms.

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NCT ID: NCT00092521 Completed - Cervical Cancer Clinical Trials

Cervical Intraepithelial Neoplasm (CIN)-Warts Efficacy Trial in Women (Gardasil)(V501-013)(COMPLETED)

Start date: December 2001
Phase: Phase 3
Study type: Interventional

The primary purpose of the study is to determine if GARDASIL (V501) with four components is able to prevent cervical cancer, cervical dysplasia, including Cervical Intraepithelial Neoplasia (CIN)(Any Grade) and Adenocarcinoma In Situ (AIS), and genital warts.

NCT ID: NCT00092495 Completed - Cervical Cancer Clinical Trials

Study of an Investigational Vaccine in Pre-Adolescents and Adolescents (Gardasil)(V501-016)

Start date: December 2002
Phase: Phase 3
Study type: Interventional

The primary purpose of the study is to determine if an investigational vaccine Gardasil (V501) with 4 components will provide an immune response and will be well tolerated in pre-adolescents and adolescents.

NCT ID: NCT00092482 Completed - Cervical Cancer Clinical Trials

Immunogenicity Bridge Between an Investigational Monovalent Vaccine and the Equivalent Component of Gardasil (V501) a Quadrivalent Vaccine (V501-012)(COMPLETED)

Start date: June 28, 2002
Phase: Phase 3
Study type: Interventional

The purpose of the study is to determine if an investigational vaccine with a single component develops an immune response that is similar to the equivalent investigational vaccine with four components to reduce cervical disease.

NCT ID: NCT00091130 Completed - Cervical Cancer Clinical Trials

SGN-00101 Vaccine in Treating Human Papillomavirus in Patients Who Have Abnormal Cervical Cells

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

This randomized phase II trial is studying how well SGN-00101 vaccine works compared to a placebo in treating human papillomavirus and preventing cervical cancer in patients with abnormal cervical cells. Vaccines, such as SGN-00101, may make the body build an immune response to kill human papillomavirus and abnormal cervical cells and may be effective in preventing cervical cancer

NCT ID: NCT00087126 Completed - Cervical Cancer Clinical Trials

Topotecan in Treating Women With Persistent or Recurrent Cervical Cancer

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

RATIONALE: Drugs used in chemotherapy, such as topotecan, work in different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: This phase II trial is studying how well topotecan works in treating women with persistent or recurrent cervical cancer.

NCT ID: NCT00087113 Completed - Cervical Cancer Clinical Trials

Pemetrexed Disodium in Treating Patients With Recurrent Cancer of the Cervix

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

RATIONALE: Drugs used in chemotherapy, such as pemetrexed disodium, work in different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: This phase II trial is studying how well pemetrexed disodium works in treating patients with recurrent cancer of the cervix.

NCT ID: NCT00086242 Completed - Cervical Cancer Clinical Trials

Telephone Counseling or Standard Care in Patients Who Have Completed Treatment for Stages I, II, or III Cervical Cancer

Start date: August 1, 2004
Phase: N/A
Study type: Interventional

RATIONALE: Telephone counseling after treatment may reduce stress and improve the well-being and quality of life of patients who have cervical cancer. Changes in quality of life may be related to changes in immune function and neuroendocrine function. PURPOSE: This randomized phase I trial is studying how well telephone counseling works compared to standard care in reducing stress in patients who have completed treatment for stage I, stage II, or stage III cervical cancer.

NCT ID: NCT00084903 Completed - Cervical Cancer Clinical Trials

Fluorescence and Reflectance Spectroscopy During Colposcopy in Detecting Cervical Intraepithelial Neoplasia and Dysplasia in Healthy Participants With a History of Normal Pap Smears

Start date: April 1998
Phase: N/A
Study type: Interventional

RATIONALE: New diagnostic procedures such as fluorescence and reflectance spectroscopy (shining light on tissue and measuring patterns of light reflected) may improve the ability to noninvasively detect cervical intraepithelial neoplasia and dysplasia. PURPOSE: This diagnostic trial is studying how well fluorescence and reflectance spectroscopy during colposcopy work in detecting cervical intraepithelial neoplasia and dysplasia in healthy participants with a history of normal Pap smears.

NCT ID: NCT00084123 Completed - Cervix Neoplasms Clinical Trials

Healing Touch and Relaxation Therapies in Cervical Cancer Patients

Start date: September 2002
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effects of healing touch and relaxation therapy on cervical cancer patients undergoing chemotherapy and radiation treatment.

NCT ID: NCT00081263 Completed - Cervical Carcinoma Clinical Trials

Celecoxib in Treating Patients With Cervical Intraepithelial Neoplasia

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

This randomized phase II trial studies how well celecoxib works in treating patients with cervical intraepithelial neoplasia, a precancerous lesion of the cervix which can develop into cervical cancer. Celecoxib may be effective in preventing the development of cervical cancer in patients who have cervical intraepithelial neoplasia.