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Gynecologic Neoplasms clinical trials

View clinical trials related to Gynecologic Neoplasms.

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NCT ID: NCT03101280 Completed - Clinical trials for Gynecologic Neoplasms

A Combination Study of Rucaparib and Atezolizumab in Participants With Advanced Gynecologic Cancers and Triple-Negative Breast Cancer

Start date: April 27, 2017
Phase: Phase 1
Study type: Interventional

This is a Phase Ib, open-label, non-randomized study in patients with previously treated advanced ovarian or endometrial cancer (Part 1) and platinum-sensitive ovarian cancer or triple-negative breast cancer (TNBC) (Part 2) to investigate the dose, safety, pharmacokinetics, and preliminary efficacy of rucaparib in combination with atezolizumab. The study is conducted in 2 parts: a Dose-Finding Phase (Part 1) and a Dose-Expansion Phase (Part 2)

NCT ID: NCT02935530 Completed - Clinical trials for Venous Thromboembolism

Thromboprophylaxis After Surgery for Gynecologic Malignancy in China

Start date: January 2016
Phase: Phase 3
Study type: Interventional

Venous thromboembolism (VTE) is an important cause of post-operative morbidity and mortality in women undergoing surgery for gynecologic malignancies. Although the benefit of thromboprophylaxis in reduction of post-operative VTE events after surgery for gynecologic cancers has been well documented around the world, the evidence for Chinese women is rare. The investigators designed this prospective and randomized study to assess the benefit of pharmacologic prophylaxis for patients received surgical treatment for gynecologic malignancies in China.

NCT ID: NCT02918461 Completed - Cognition Disorders Clinical Trials

Emerging From the Haze for Gynecologic Cancer Survivors

Start date: January 10, 2017
Phase: N/A
Study type: Interventional

At Cedars-Sinai Medical Center, the investigators have developed a novel curriculum for a 6-week psycho-educationally-based, cognitive behavioral program to help patients with subjective cognitive complaints after cancer treatment, titled Emerging from the Hazeā„¢ (Haze). Each series meets once a week for 2-2.5 hours for 6 weeks. The objective of this study is to quantify the impact of a trainee-taught Emerging from the Haze course on gynecologic cancer survivors' self-report of cognitive changes based on the change of FACT-Cog score.

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: 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: 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: NCT02309944 Completed - Obesity Clinical Trials

Negative Pressure Wound Therapy in Obese Gynecologic Oncology Patients

Start date: May 2015
Phase: N/A
Study type: Interventional

The purpose of the study is to test whether the use of a new wound closure technique can decrease the rates of wound complications in obese cancer patients.