Clinical Trials Logo

Genital Neoplasms, Female clinical trials

View clinical trials related to Genital Neoplasms, Female.

Filter by:

NCT ID: NCT02786524 Completed - Ovarian Neoplasms Clinical Trials

Effect of Outpatient Symptom Management on Gynecologic Oncology Patients Receiving Chemotherapy

Start date: February 15, 2016
Phase: N/A
Study type: Interventional

To evaluate whether formal referral to The Symptom Management and Supportive Care Clinic improves symptom burden in advanced stage or recurrent gynecologic oncology chemotherapy patients compared with symptom management performed by the primary gynecologic oncologist.

NCT ID: NCT02781155 Recruiting - Breast Neoplasms Clinical Trials

Limiting Chemotherapy Side Effects by Using Moxa

Start date: February 2016
Phase: Phase 1/Phase 2
Study type: Interventional

This study investigates whether it is feasible to teach cancer patients undergoing chemotherapy to self-administer daily moxibustion to reduce chemotherapy side effects. Moxibustion is a therapy used in traditional Chinese medicine that uses heat.

NCT ID: NCT02774759 Active, not recruiting - Clinical trials for Malignant Neoplasms of Female Genital Organs

Feasibility of the NEXT Steps Weight Loss Intervention +/- Resistance Training for Endometrial Cancer Survivors: Effect on Lean Mass & Biomarkers

Start date: October 17, 2016
Phase: N/A
Study type: Interventional

The goal of this research study is to learn if a home-based physical activity program is feasible and can help endometrial cancer survivors lose weight.

NCT ID: NCT02740114 Terminated - Gynecologic Cancer Clinical Trials

Wound Infiltration With Liposomal Bupivacaine vs. Standard Wound Infiltration With Bupivacaine in Patient's Undergoing Open Gynecologic Surgery on an Enhanced Recovery Pathway

Start date: August 31, 2016
Phase: Phase 3
Study type: Interventional

Bupivacaine is a drug that is traditionally given as an injection to numb surgical sites. Liposomes are molecules that are similar to fats. Sometimes drugs are combined with liposomes to make them able to stay in the body for longer periods of time. This has been done with bupivacaine to create liposomal bupivacaine. The goal of this clinical research study is to compare the effects of bupivacaine to those of liposomal bupivacaine when given to patients who are having gynecologic surgery. Researchers want to compare how long the drugs work to numb the wound and how long patients take to recover from surgery.

NCT ID: NCT02728999 Terminated - Clinical trials for Benign Female Reproductive System Neoplasm

Does Less Trendelenburg Make a Difference in Robotic Assisted Gynecological Procedures?

Start date: June 2013
Phase: N/A
Study type: Interventional

Patient/Population: Women over the age of 18, who are not pregnant and are undergoing benign, robotic-assisted gynecologic procedures at Lutheran General Hospital. Intervention: Decreasing the angle of Trendelenburg for the procedure Control: Steep Trendelenburg, which is the usual standard of care, to the limit of the operative bed, which is 30 degrees. Outcome: Outcomes will include the mean angle of Trendelenburg in the experimental arm and the difference in Trendelenburg between the two arms. Additional outcomes included will be end tidal Carbon dioxide, peak airway pressure, mean arterial pressure, heart rate and arterial Carbon dioxide. Secondary outcomes will include operative time, blood loss and conversion to laparotomy.

NCT ID: NCT02728830 Completed - Clinical trials for Fallopian Tube Cancer

A Study of Pembrolizumab on the Tumoral Immunoprofile of Gynecologic Cancers

Start date: June 2016
Phase: Early Phase 1
Study type: Interventional

The ultimate goal of the study is to identify potential biomarkers, immune gene expression signatures, and co-stimulatory pathways that may be used to understand the effect of immune checkpoint inhibitors on gynecologic cancers.

NCT ID: NCT02714439 Active, not recruiting - Clinical trials for Malignant Neoplasms of Female Genital Organs

Low-Cost Imaging for Cervical Cancer Prevention in the Texas Lower Rio Grande Valley

Start date: October 25, 2016
Phase: Early Phase 1
Study type: Interventional

The purpose of this study is to evaluate a different type of medical equipment called "High-Resolution Microendoscope" (HRME) for the diagnosis of cervical pre-cancerous lesions and cervical cancer. The investigators want to compare patients' clinical findings using the current equipment used in clinic with the clinical findings using new equipment we are testing on this research project. If the new equipment is proven to give comparable findings with current equipment being used, doctors might be able to offer a diagnosis and treat cervical lesions in one visit. It might not be necessary to wait for cervical biopsies to come back before women would receive the indicated treatment. Study subjects are being asked to participate because they have been diagnosed with an abnormal Papanicolaou (Pap) PAP smear, positive human papillomavirus (HPV) test or history of cervical dysplasia and need to have a colposcopic examination to determine the reason for abnormal results and receive treatment.

NCT ID: NCT02653469 Completed - Clinical trials for Gynecologic Neoplasms

Augmented Pulse Pressure Variation to Predict Fluid Responsiveness in Open Laparotomy

Start date: September 2015
Phase: N/A
Study type: Observational

Pulse pressure variation (PPV) is a well-known and widely used dynamic preload indicator based on heart-lung interaction to predict fluid responsiveness. Generally, patients are considered to be fluid-responsive when the PPV value larger than 11-13%. However, several previous researches demonstrated that there is a zone of uncertainty (grey zone) in PPV. To predict fluid-responsiveness accurately in the patients with PPV within grey zone (9-13%), the investigators would evaluate the augmented PPV using augmented ventilation.

NCT ID: NCT02609880 Completed - Pain Clinical Trials

Cognitive Behavioral Effects on Sleep, Pain, and Cytokines in Gynecologic Cancer

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

Gynecologic cancers cause substantial morbidity and mortality among women. Developing, implementing, and disseminating interventions that reduce morbidity and mortality secondary to gynecologic cancers are a public health priority. In spite of this, there is a paucity of research examining the effects of psychosocial interventions on patient-centered and physiological outcomes in this population. To the extent that psychological factors may influence quality of life and tumor biology among women with gynecologic cancers, psychological interventions may represent an important adjunct to standard clinical care in this population. As such, this study will examine the effects of a psychosocial intervention on sleep, pain, mood, cortisol, and cytokines in women with gynecologic cancers.

NCT ID: NCT02518308 Completed - Depression Clinical Trials

Mindfulness Intervention in Reducing Anxiety in Patients Who Have Been Treated for Gynecologic Cancer

Start date: November 18, 2015
Phase: N/A
Study type: Interventional

This pilot clinical trial studies how well a mindfulness-based stress reduction (MBSR) intervention works in reducing anxiety in patients who have undergone treatment for gynecologic cancer but no longer have any sign of disease. Gynecologic cancer is cancer of the female reproductive tract, which includes the cervix, endometrium, fallopian tubes, ovaries, uterus, and vagina. Side effects from treatment for these cancers may include anxiety, fatigue, depression, and sexual function changes. Mindfulness training uses meditation and yoga to help patients focus on breathing, bodily sensations, and mental awareness. This may help decrease patients' stress and anxiety and improve their quality of life, and may also help their immune system.