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Cervical Cancer clinical trials

View clinical trials related to Cervical Cancer.

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NCT ID: NCT01710085 Recruiting - Cervical Cancer Clinical Trials

Value of Diffusion Weighted Magnetic Resonance Imaging in Detection of Recurrent Disease in Surgically Treated Cervical and Endometrial Cancer Patients

Start date: August 2012
Phase: N/A
Study type: Interventional

Endometrial and cervical cancers are one of the most common malignancies seen in females. Identification of recurrent disease in early phases of treatment carries a primary importance on the outcome of patients. Diffusion-weighted magnetic resonance imaging (DWI) is a new technique recently started to be performed in body imaging and has potential ability to detect recurrent disease. The aim of this study is to investigate the diagnostic impact of DWI in detection of recurrent disease in patients treated with curative surgery in endometrial and cervical cancer.

NCT ID: NCT01709175 Completed - Breast Cancer Clinical Trials

Strength Training Study for Survivors of Breast and Gynecologic Cancer

Start date: November 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to compare once-a-week vs. twice-a-week strength training in survivors of breast and gynecologic cancer to determine which is the optimal exercise prescription.

NCT ID: NCT01706705 Completed - Cervical Cancer Clinical Trials

Magnetic Resonance Imaging (MRI) Brachytherapy Applicator Study

Start date: October 22, 2012
Phase: N/A
Study type: Interventional

The goal of this clinical research study is to learn if computed tomography (CT) and magnetic resonance imaging (MRI) images can better help to plan internal radiation treatment.

NCT ID: NCT01705288 Completed - Ovarian Cancer Clinical Trials

Implementation of a Rapid Recovery Program in Gynecologic Oncology Surgery: A Pilot Study

Start date: January 1, 2013
Phase: Early Phase 1
Study type: Interventional

Over 600,000 hysterectomies are performed annually in the United States. Despite increasing use of less invasive approaches, the majority of hysterectomies are still performed via traditional laparotomy, which can be associated with generally slower recovery and longer lengths of post-operative hospitalization. Rapid Recovery Protocols (RRP) seek to optimize post-surgical morbidity outcomes by returning a patient to normal physiology as quickly as possible following surgery.

NCT ID: NCT01704235 Completed - Cervical Cancer Clinical Trials

Vietnamese Women's Health Project III

Start date: November 30, 2012
Phase:
Study type: Observational

The purpose of this protocol is to understand the extent of symptom perception and preventive care-seeking among Vietnamese American women and their impact on cervical cancer screening from the perspectives and experiences of key informants including primary health care providers and Vietnamese American women (VAW, foreign-born and United States-born). With this information, the investigators can better understand how to promote cervical cancer screening in the Vietnamese community.

NCT ID: NCT01691144 Completed - Ovarian Cancer Clinical Trials

Follow-up of Gynecological Cancer Patients, Their Needs and Expectations, A Cooperation Project

Start date: September 2012
Phase: N/A
Study type: Observational

Follow-up of cancer patients accounts for a substantial part of outpatient activity, and alternative models of care are developing. In some countries, low-risk follow-up is already done in primary care, mainly in breast, and colorectal cancer. In this study the investigators will explore gynecological cancer patients about their expectations regarding their future follow-up plan. Further, the investigators will ask about the experience and satisfaction among patients who have already attended a follow-up programme for 2-3 years. In addition, the investigators will especially focus on the cooperation aspect between primary and secondary care. The investigators hypothesize that follow-up of selected gynecological cancer patients can be done by general practitioners.

NCT ID: NCT01680523 Recruiting - Cervical Cancer Clinical Trials

Radical Hysterectomy Followed by Tailored Adjuvant Therapy Versus Primary Chemoradiation Therapy in Bulky Early-stage Cervical Cancer (KGOG 1029)

Start date: September 2012
Phase: N/A
Study type: Interventional

To compare 5-year overall survival between patients who undergo radical hysterectomy followed by tailored adjuvant therapy and patients who receive primary chemoradiation therapy in FIGO stage IB2 and IIA2 cervical cancer

NCT ID: NCT01679483 Completed - Ovarian Cancer Clinical Trials

Efficacy Study of FloSeal for Prevention of Lymphocele After Lymphadenectomy for Gynecologic Cancer

Start date: September 2012
Phase: N/A
Study type: Interventional

To compare the incidence of lymphocele and lymphatic ascites between patient who use versus who do not use FloSeal during lymph node dissection

NCT ID: NCT01673022 Completed - Cervical Cancer Clinical Trials

Determining the Sensitivity of Sentinel Lymph Nodes Identified With Robotic Fluorescence Imaging

FIRES
Start date: May 2012
Phase: N/A
Study type: Interventional

Description: This is a multi-institutional study investigating the sensitivity and negative predictive value of sentinel lymph nodes mapped with robotic assisted near infrared imaging after cervical injection of indocyanine green (ICG) dye for women with stage I endometrial or cervical cancer at the time of their robotic surgical staging. Patients will receive cervical injection of 1mg ICG after induction of anesthesia followed by sentinel lymph node mapping using robotic assisted fluorescence imaging. The sentinel lymph nodes identified will be removed and sent for ultraprocessing by pathology. The non-sentinel pelvic and para-aortic (if indicated) non-sentinel nodes will be removed and sent for routine pathologic processing according to standard of care for these surgical procedures. The pathologic results of the sentinel and non-sentinel nodes will be evaluated for sensitivity and negative predictive value in their ability to detect metastatic disease.

NCT ID: NCT01672892 Completed - Cervical Cancer Clinical Trials

Standard Versus Intensity-Modulated Pelvic Radiation Therapy in Treating Patients With Endometrial or Cervical Cancer

Start date: November 2012
Phase: Phase 3
Study type: Interventional

RATIONALE: Radiation therapy uses high-energy x-rays and other types of radiation to kill tumor cells. Specialized radiation therapy that delivers a high dose of radiation directly to the tumor may kill more tumor cells and cause less damage to normal tissue. PURPOSE: This randomized phase III trial is studying two different methods of radiation and their side effects and comparing how well they work in treating endometrial and cervical cancer after surgery.