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Ovarian Cancer clinical trials

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NCT ID: NCT00511641 Active, not recruiting - Ovarian Cancer Clinical Trials

Quality of Life Associated With a Low-Risk Screening Program for Ovarian Cancer

Start date: February 12, 2002
Phase:
Study type: Observational

The goal of this research study is to learn more about how women feel about an ovarian cancer screening program that involves getting a blood test to measure CA 125 levels. This includes finding out about women's quality of life and whether they are concerned or worried about their risk of developing cancer. This study also seeks to find out whether elevated CA 125 levels affect participants in terms of cancer worries or concerns.

NCT ID: NCT00510653 Completed - Ovarian Cancer Clinical Trials

Gleevec Study for Patients With Ovarian Cancer

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

Primary Objectives: 1. To determine the efficacy of Gleevec in patients with recurrent platinum-resistant, taxane-resistant epithelial ovarian cancer, primary peritoneal cancer, or fallopian tube cancer whose tumor expresses either c-KIT, platelet-derived growth factor receptor (PDGRF), or ABL. 2. To determine the nature and degree of toxicity of Gleevec in this cohort of patients.

NCT ID: NCT00508378 Completed - Ovarian Cancer Clinical Trials

Chemotherapy-Related Toxicities In Ovarian Cancer Patients

Start date: January 2001
Phase:
Study type: Observational

Primary Objectives: 1. To assess the preferences of women with ovarian cancer, their clinical caregivers, familial caregivers, and a control group for toxicities associated with chemotherapy. - To compare preferences of women with ovarian cancer to preferences of their clinical caregivers. - To compare preferences of women with ovarian cancer to preferences of their familial caregivers. - To compare preferences of women with ovarian cancer to preferences of a women in the control group. 2. To prospectively collect quality of life data from women with ovarian cancer. 3. To prospectively collect symptom assessment data from women with ovarian cancer.

NCT ID: NCT00507741 Completed - Ovarian Cancer Clinical Trials

Study of Vintafolide (MK-8109, EC145) in Participants With Advanced Ovarian and Endometrial Cancers (MK-8109-007, EC-FV-02)

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

This is a Phase II clinical trial evaluating the benefit from therapy with vintafolide in participants with advanced ovarian and endometrial cancers.

NCT ID: NCT00505661 Terminated - Ovarian Cancer Clinical Trials

Letrozole in Patients With Ovarian Tumors

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

Primary Objectives: - To determine the objective response rate of Letrozole when administered to patients with advanced or recurrent borderline tumors or low-grade epithelial cancers from the ovary , fallopian tube or peritoneum. - To determine the time to tumor progression of patients with advanced or recurrent borderline tumors or low-grade epithelial cancers from the ovary, fallopian tube or peritoneum. - To identify the biological markers to predict response to Letrozole and study the aspects of the hormones in these types of tumors.

NCT ID: NCT00504257 Completed - Ovarian Cancer Clinical Trials

Avastin in Combination With Docetaxel in Ovarian/Fallopian Tube/Peritoneum Carcinoma

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

The purpose of this study is to evaluate the effectiveness of the combination of Avastin and Docetaxel in the treatment of women with platinum sensitive recurrent epithelial ovarian cancer within 12 months of platinum chemotherapy.

NCT ID: NCT00501644 Completed - Ovarian Cancer Clinical Trials

Chemoimmunotherapy Study for Patients With Epithelial Ovarian Cancer

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

Primary Objectives: 1. Determine response rate, time to progression, and toxicity of a schedule of carboplatin by IV (intravenous) infusion, GM-CSF and rIFN-g by SC (subcutaneous injection) in patients with potentially platinum-sensitive recurrent Müllerian carcinomas. 2. Determine whether this treatment schedule is associated with: 1. increased levels of monocytes (>2-fold and absolute numbers 1000 cells/ml,) and of LN-DR+ DC (CD11c+ and CD123+ subsets) 2. induction of priming and activation of MO/MA (monocytes/ macrophages), and maturation of DC (dendritic cells). 3. Determine the toxicity profile of consolidation treatment with IP (intraperitoneal) injections of rIFN-g added to carboplatin (IV) and GM-CSF (SC) for 4 doses/course. 4. Determine the effects of carboplatin plus GM-CSF and rIFN-g on quality of life in patients with platinum-sensitive Müllerian carcinomas. 5. To begin an exploration of cell surface proteins on purified activated peripheral blood and ascites monocyte/macrophages both before and after treatment with GM-CSFand rIFN-g.

NCT ID: NCT00499512 Active, not recruiting - Ovarian Cancer Clinical Trials

Role of Spirituality in Coping and Surviving With Ovarian Cancer, Primary Peritoneal or Fallopian Tube Cancer

Start date: August 10, 2005
Phase:
Study type: Observational

The goal of this psychosocial research study is to examine and explain the influence of spirituality on patients with ovarian, primary peritoneal or fallopian tube cancer.

NCT ID: NCT00496106 Completed - Ovarian Cancer Clinical Trials

Stress, Immunity and Cervical Cancer: Biobehavioral Outcomes

CXR01
Start date: August 2007
Phase: N/A
Study type: Interventional

The purpose of the study is to: 1. Test the efficacy of psychosocial telephone counseling (PTC) for cervical cancer survivors, compared to usual care. 2. Evaluate the longitudinal immune and neuroendocrine parameters in cervical cancer patients who have received PTC, compared to usual care. 3. Examine the longitudinal relationship between PTC associated modulations of quality of life (QOL) measures and biologic parameters (immune and neuroendocrine).

NCT ID: NCT00489359 Completed - Ovarian Cancer Clinical Trials

Trial of Pemetrexed and Carboplatin in Patients With Recurrent Ovarian or Primary Peritoneal Cancer

Start date: July 2005
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine efficacy of the combination therapy of pemetrexed and carboplatin as treatment for patients with platinum-sensitive ovarian cancer. This study also includes patients with primary peritoneal cancer.