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Ovarian Cancer clinical trials

View clinical trials related to Ovarian Cancer.

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NCT ID: NCT02307500 Completed - Ovarian Cancer Clinical Trials

Regorafenib in Patients With Metastatic Solid Tumors Who Have Progressed After Standard Therapy

RESOUND
Start date: December 2014
Phase: Phase 2
Study type: Interventional

This is a single arm, single-stage, phase II trial to evaluate the activity of Regorafenib in patients with metastatic solid tumors (pancreatic cancer, ovarian cancer, melanoma, sarcoma, thymoma (type B2 - B3) and thymic carcinoma, who have progressed after standard therapy.

NCT ID: NCT02305498 Completed - Breast Cancer Clinical Trials

Yoga Practice for Breast or Ovarian Cancer Patients

Start date: November 24, 2014
Phase: N/A
Study type: Interventional

Previous research suggests that regular physical activity may make cancer survivors do better in the long run. Laboratory studies suggest that stress may be bad for cancer patients as well. The investigators are interested in whether yoga, a practice that combines physical activity and stress reduction, is beneficial to cancer survivors. To answer that question, the investigators will need to do a large scale clinical trial. Before the investigators can do that large study, they need to know whether people are willing to participate in this kind of study, whether they can do the yoga practice regularly and for how long, what kind of changes they may experience in how they can handle their daily activities, emotion, sleep, memory and problem solving ability, and what are the changes that can happen in their body after doing the yoga practice. Answering these questions is what this study is about.

NCT ID: NCT02298855 Completed - Ovarian Cancer Clinical Trials

Individualised Versus Conventional Medical Follow-up for Women After Primary Treatment for Ovarian Cancer.

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

The purpose of this study in women who have completed primary treatment for ovarian cancer is to investigate the effects of individualised follow-up care delivered by a nurse compared to conventional medical follow-up on quality of life and mood. The investigators aim to determine if the individualised treatment is acceptable to women compared to the conventional treatment.

NCT ID: NCT02297958 Completed - Ovarian Carcinoma Clinical Trials

Impact of Fas/FasL in Chemotherapy Response in Epithelial Ovarian Carcinoma

IFFaLCCO
Start date: January 15, 2015
Phase:
Study type: Observational

Ovarian carcinoma has poor prognosis and new therapeutic strategies are required. Many patients with ovarian carcinoma showed resistance to chemotherapy. Cleaved FasL is known for induced atypical response when is binding to Fas such as avoiding apoptosis and inducing cell motility.

NCT ID: NCT02288676 Recruiting - Ovarian Cancer Clinical Trials

DOvEEgene: Diagnosing Ovarian and Endometrial Cancer Early Using Genomics

DOvEEgene
Start date: January 2014
Phase:
Study type: Observational

This study aims to develop and validate a test for diagnosing ovarian and endometrial cancers early. It relies on detecting somatic mutations that are associated with these cancers in a biofluids sample taken from the cervix and the uterine cavity.

NCT ID: NCT02287519 Completed - Ovarian Cancer Clinical Trials

Sexual Therapy and Rehabilitation After Treatment for Ovarian Cancer (START-OC): A Pilot Intervention

START-OC
Start date: November 2014
Phase: N/A
Study type: Interventional

This research study is evaluating an educational intervention for women who have experienced changes in sexual function after treatment for ovarian cancer.

NCT ID: NCT02278783 Terminated - Ovarian Cancer Clinical Trials

Phase 2 Trial of Regorafenib in Patients With Recurrent Ovarian, Primary Peritoneal and Fallopian Tube Cancer

Start date: March 2015
Phase: Phase 2
Study type: Interventional

This will be a non-blinded, single arm study to test the efficacy of Regorafenib in patients with recurrent ovarian, primary peritoneal, and fallopian tube cancer.

NCT ID: NCT02269293 Completed - Ovarian Cancer Clinical Trials

Selective Inhibitor of Nuclear Export, Selinexor (KPT-330) in Combination With Paclitaxel and Carboplatin in Patients With Advanced Ovarian or Endometrial Cancers

Start date: October 13, 2014
Phase: Phase 1
Study type: Interventional

The purpose of this study is to test the safety of the investigational drug, selinexor (KPT-330), in combination with carboplatin and paclitaxel chemotherapy, where paclitaxel will be given at two different dosing schedules and selinexor will be given at two different dosing schedules. Carboplatin and paclitaxel chemotherapy is a commonly used therapy for the treatment of advanced or recurrent ovarian, fallopian tube, primary peritoneal, or endometrial cancer. The investigators want to find out what effects, good and/or bad, selinexor has on the patient and the cancer.

NCT ID: NCT02262455 Completed - Ovarian Cancer Clinical Trials

Effects of STM 434 Alone or in Combination With Liposomal Doxorubicin in Patients With Ovarian Cancer or Other Advanced Solid Tumors

Start date: October 2014
Phase: Phase 1
Study type: Interventional

This is a Phase I study to test the safety, pharmacokinetics and effectiveness of STM 434 alone, or in combination with liposomal doxorubicin, in patients with ovarian cancer or other advanced solid tumors.

NCT ID: NCT02258165 Completed - Clinical trials for Ovarian Cancer Stage IV

Impact of Gated PET/CT in the Diagnosis of Advanced Ovarian Cancer

IMAGE
Start date: February 2015
Phase:
Study type: Observational

This study will be the first prospective study enrolling consecutive patients with advanced ovarian cancer to determine the prevalence of thoracic and extra-abdominal involvement in this patient group and the relative value of gated PET and CT for diagnosing extra-abdominal involvement. This study will also answer a number of other stil unanswered questions: the impact of gating and the impact of gated PET on clinical management of patients with advanced ovarian cancer. This study also individualises patients' treatment to allow patients who may benefit most form optimal surgical cytoreduction and those who are better treated by neoadjuvant