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Gynecological Cancers clinical trials

View clinical trials related to Gynecological Cancers.

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NCT ID: NCT04760327 Recruiting - Clinical trials for Gynecological Cancers

Electrochemotherapy of Gynecological Cancers

GynECT
Start date: July 1, 2020
Phase: Phase 2
Study type: Interventional

To determine the effectiveness, feasibility and safety of electrochemotherapy in treatment of local and/or regional recurrences of gynecological cancers with electrochemotherapy in which standard treatment options have been exhausted.

NCT ID: NCT03470870 Recruiting - Clinical trials for Gynecological Cancers

Nomogram Control of Predictive Factors of Early Withdrawal After Gynecologic Oncology Surgery in the Enhanced Recovery After Surgery (ERAS) Protocol and Assessment of Practices

NomogramGyneco
Start date: January 8, 2018
Phase:
Study type: Observational

Validation of a predictive nomogram of a short hospital stay (less than two days after surgery) on a prospective cohort of patients.

NCT ID: NCT01793545 Completed - Endometrial Cancer Clinical Trials

Endometrial Cancer Testing With Vaginal and Endometrial Cell Samples

Start date: February 11, 2013
Phase:
Study type: Observational

Background: - Endometrial cancer is one of the most common gynecologic cancers. If it is caught at an early stage, it can be treated more easily. Women who have this type of cancer often have a history of irregular menstrual bleeding. They may also have abnormal findings during gynecologic exams. Pap smears and cervical cell collection may be able to collect cell samples for cancer testing. However, samples from the vagina or endometrium may produce more accurate results. Researchers want to collect vaginal and endometrial cell samples to improve their tests for and understanding of endometrial cancer. Objectives: - To collect vaginal and endometrial cell samples to study endometrial cancer. Eligibility: - Women at least 18 years of age who have had symptoms of abnormal uterine or post-menopausal bleeding, or abnormal ultrasound findings. Design: - Participants will be screened with a physical exam and medical history. - Participants will have a pelvic exam. Before the exam, they will insert a small tampon in the vagina. The tampon will stay in place for about 10 to 30 minutes. The tampon will then be removed and collected for the study. - During the pelvic exam, tissue will be collected from the uterine lining with a special brush. An additional sample (biopsy) will be collected from the lining. - A blood sample will also be collected as part of the study.

NCT ID: NCT01505400 Active, not recruiting - Breast Cancer Clinical Trials

Integrated Molecular Profiling in Advanced Cancers Trial

IMPACT
Start date: February 2012
Phase:
Study type: Observational

Substantial progress has been made in the treatment of cancer through the use of targeted therapies, but what works for one patient might not work for another patient. Certain drugs are now being developed that target specific molecules in the body that are believed to be part of the disease. Biomarkers are specific characteristics of the cancer that may help provide prognostic information (i.e. how well patients will be regardless of the treatments given) or help predict sensitivity or resistance to a specific treatment. The study will collect archival tumor samples (previously collected biopsy or surgical tumor samples) to provide biomarker data about a patient's cancer, in order to help their physicians to identify which clinical trials of molecularly targeted therapies may be most appropriate for the patient in the future.

NCT ID: NCT00984321 Active, not recruiting - Breast Cancer Clinical Trials

A Pilot Study of Geriatric Specific Interventions for Quality of Life in Elderly Patients With Cancer

Start date: September 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to examine whether psychoeducation counseling for older cancer patients undergoing treatment is feasible and worthwhile. The investigators will test this in a group or individual phone counseling format. Many cancer patients seek counseling to help with the emotional burden of their illnesses. Counseling often helps them cope with cancer by giving them a place to express their feelings. This geriatric-specific psychoeducation is intended to help older cancer patients cope with the burden of cancer and aging. The purpose of this study is to see if this type of counseling helps reduce depressive symptoms, anxiety, perception of loneliness and isolation. In addition this counseling aims to improve coping and quality of life (QOL). Individuals who choose not to take part in the intervention study will be asked if they are willing to participate in a brief refusal sub study. The purpose of the refusal substudy is to compare levels of distress in patients that choose to participate and those that decline. This will yield valuable data that will help us distinguish between patients that decline due to lack of interest in research and those that decline due to high levels of distress. Participation in the refusal sub study consists of completion of 2 brief questionnaires.