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Vulvar Neoplasms clinical trials

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NCT ID: NCT00545792 Completed - Ovarian Cancer Clinical Trials

Safety Study Of Avastin And Pelvic Radiation In Women With Recurrent Gynecological Cancers

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

This research study is evaluating a drug called avastin in combination with standard radiation as a possible treatment for treatment for recurrent pelvic-confined gynecological cancer (i.e. endometrial, cervical, vulvar, ovarian or vaginal cancers).

NCT ID: NCT00543543 Completed - Cervical Cancer Clinical Trials

Broad Spectrum HPV (Human Papillomavirus) Vaccine Study in 16-to 26-Year-Old Women (V503-001)

Start date: September 24, 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study was to evaluate the safety, efficacy, and immunogenicity of V503 in comparison to GARDASIL. The primary hypotheses tested in the study were 1) V503 administered to 16- to 26-year-old adolescents and young women is generally well-tolerated, 2) V503 reduces combined incidence of Human Papillomavirus (HPV) Type 31/33/45/52/58-related disease compared with GARDASIL, and 3) V503 induces non-inferior geometric mean titers for HPV Type 6/11/16/18 antibodies compared with GARDASIL.

NCT ID: NCT00520598 Completed - Cervical Cancer Clinical Trials

Broad Spectrum HPV (Human Papillomavirus) Vaccine in 16 to 26 Year Old Women (V505-001)

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

The purpose of this study is to evaluate the safety and immunogenicity of V505 in comparison to GARDASIL (TM)

NCT ID: NCT00504023 Completed - Vulvar Cancer Clinical Trials

Topical Imiquimod in Treating Patients With Recurrent Paget's Disease of the Vulva

Start date: April 2007
Phase: N/A
Study type: Interventional

RATIONALE: Biological therapies, such as imiquimod, may stimulate the immune system in different ways and stop tumor cells from growing. Applying topical imiquimod to the vulva may be an effective treatment for recurrent Paget's disease. PURPOSE: This clinical trial is studying how well topical imiquimod works in treating patients with recurrent Paget's disease of the vulva.

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: NCT00335998 Completed - Clinical trials for Recurrent Ovarian Epithelial Cancer

Phase I Study of Intravenous Triapine (IND # 68338) in Combination With Pelvic Radiation Therapy With or Without Weekly Intravenous Cisplatin Chemotherapy for Locally Advanced Cervical, Vaginal, or Pelvic Gynecologic Malignancies

Start date: March 2006
Phase: Phase 1
Study type: Interventional

Drugs used in chemotherapy, such as 3-AP and cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. 3-AP may also stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Radiation therapy uses high-energy x-rays to kill tumor cells. 3-AP and cisplatin may make tumor cells more sensitive to radiation therapy. Giving 3-AP and external-beam radiation therapy together with cisplatin may kill more tumor cells. This phase I trial is studying the side effects and best dose of 3-AP when given together with external-beam radiation therapy with or without cisplatin in treating patients with gynecologic cancer

NCT ID: NCT00315159 Completed - Vulvar Cancer Clinical Trials

Conservative Management With Isolated Sentinel Lymph Node Biopsy in Vulvar Cancer Patients.

Start date: August 2003
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate a less invasive procedure for the evaluation of the inguinal (groin) nodes in patients with a primary squamous cell carcinoma of the vulva. Each patient will undergo a sentinel lymph node dissection as well as resection of the primary tumor on the vulva. Patients who are determined to have sentinel nodes that are negative for metastatic disease will not receive a full groin dissection. Patients who have sentinel lymph nodes that contain metastasis will undergo a complete inguinal dissection. The study will evaluate the long-term outcomes in patients who receive only a sentinel lymph node dissection without a complete dissection. All patients entered onto the study will have a biopsy proven squamous cell carcinoma of the vulva. Each patient will be enrolled by a Gynecologic Oncologist practicing out of Women & Infants Hospital

NCT ID: NCT00288821 Completed - Ovarian Neoplasms Clinical Trials

Diagnostic Imaging of Lymph Nodes in Gynaecologic Oncology

Start date: February 2006
Phase: N/A
Study type: Observational

The purpose of the study is to determine the diagnostic accuracy of a new magnetic resonance imaging (MRI) technique, the diffusion weighted imaging with body background signal suppression (DWIBS) in the detection of lymph node pathology in patients with gynaecologic malignancies.

NCT ID: NCT00287885 Completed - Ovarian Cancer Clinical Trials

Docetaxel in Treating Patients With Refractory or Recurrent Advanced Gynecologic Cancer

Start date: March 2004
Phase: Phase 1
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as docetaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Docetaxel may also stop the growth of tumor cells by blocking blood flow to the tumor. Giving daily doses of docetaxel may kill more tumor cells. PURPOSE: This phase I trial is studying the side effects and best dose of docetaxel in treating patients with refractory or recurrent advanced gynecologic 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.