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Uterine Cervical Neoplasms clinical trials

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NCT ID: NCT02903693 Completed - Cervical Cancer Clinical Trials

Cervical Cancer in French Guiana: Screening Between 2006-2011

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

Given that cervical cancer is the second most frequent cancer among women in french guiana the aim of the study was to determine the screening rate among women living in French Guiana. Cervical smears are read in 2 laboratories which allowed us to compute screening rates per 100 women-years. overall the screening activity was 23.5-25.8 smears per 100 women-years. between 2006 and 2011 54% of women were screened. These baseline figures will allow to evaluate present efforts to increase the screening rate for this frequent cancer in French Guiana.

NCT ID: NCT02888717 Completed - Clinical trials for Advanced Cervical Cancer

Molecular Biology Analysis for Para-aortic Nodes in the Ultra-staging of Advanced Cervical Cancers

GYNOSNA
Start date: April 28, 2015
Phase: N/A
Study type: Interventional

The para-aortic lymph node involvement in the advanced stage of cervical cancer is a poor prognostic factor for overall survival. Concomitant chemo-radiotherapy has become the standard treatment for advanced cervical cancer. In case of para-aortic lymph node involvement, an extension of radiotherapy fields is recommended. A prospective multicentre study shown that the survival rate of patients with node ≤ 5 mm and which benefited from the expansion of radiotherapy fields was identical to the survival of pN0 patients. However, due to a specific disease, this technique should not be performed in all patients. It is necessary to reliably select patients with retroperitoneal lymph node involvement. For this, it is recommended that prior to the concurrent chemo-radiotherapy, nodal staging surgery with a definitive histological analysis. So we propose to use molecular diagnostic test OSNA (One Step Nucleic Acid Amplification) to improve lymph node metastasis detection sensitivity to achieve ultra-staging compared to conventional histology.

NCT ID: NCT02880007 Completed - Clinical trials for Cervical Adenocarcinoma

Dose Optimization in 3D Pulsed Dose Rate Brachytherapy for Patients With Locally Advanced Cervical Cancer

TRIDICOL
Start date: June 6, 2011
Phase: Phase 2
Study type: Interventional

This prospective phase II trial study aims to optimize the increase in dose to the target volume at high risk (85 to 90 Gy over 90% of its volume) and the intermediate target volume (60 Gy to 90 % of its volume) in 3D Pulsed Dose Rate Brachytherapy in treating patients with locally advanced cervical cancer.

NCT ID: NCT02866006 Completed - Clinical trials for Uterine Cervical Neoplasms

Safety and Tolerability Evaluation Study of BVAC-C in Patients With HPV Type 16 or 18 Positive Cervical Cancer

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

BVAC-C is an immunotherapeutic vaccine using B-Cell and Monocytes as antigen-presenting cells. This study is consists of 2 parts. Phase I is for safety evaluation, and Phase IIa is for efficacy assessment.

NCT ID: NCT02865889 Completed - Clinical trials for UTERINE CERVICAL NEOPLASMS

Cost-Effectiveness and Patients Satisfaction of Conventional vs Robotic-Assisted Laparoscopy in Gynecologic Oncologic Indications

Start date: September 2008
Phase: N/A
Study type: Observational

Laparoscopic surgery is gaining currency in the field of oncologic care, particularly for colorectal and gynecologic cancers. This innovation could be used either for staging purpose and therefore could steer global therapeutic options or for surgical management only. Increase knowledge and skills lead to an increase in the number and rate of the women this innovation could be offered. The project team observed a shift from traditional surgical management (abdominal radical surgery) towards laparoscopic with a focus on lymphadenectomy. This innovation however increases some costs (the surgical stage) but decrease some others (the post surgical stage). Foreseeing the pace of the dissemination needs to have objective and reliable data about who had access to laparoscopic surgery and who didn't (and why) and accurate assessment of related costs. This program will focus on uterine cancer (both cervix and corpus).

NCT ID: NCT02865837 Completed - Cervical Cancer Clinical Trials

Effect of Bladder Distension on Dosimetry in Brachytherapy of Cervical Cancer

VESICOL
Start date: September 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to compare, for each patient, dosimetry of organs at risk (bladder, rectum, sigmoid, small bowel) in two bladder distension procedures (emptied by a urinary catheter or filled with 120cc) during PDR 3D image-guided brachytherapy of cervical cancer.

NCT ID: NCT02865135 Completed - Clinical trials for Cancer of Head and Neck

Trial To Test Safety And Efficacy Of Vaccination For Incurable HPV 16-Related Oropharyngeal, Cervical And Anal Cancer

Start date: March 30, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

This research study is studying a therapeutic vaccine, named DPX-E7, as a possible treatment for Human Papilloma Virus or HPV related head and neck, cervical or anal cancer (positive for HLA-A*02).

NCT ID: NCT02849340 Completed - Clinical trials for Recurrent Cervical Cancer

Combination of Cryosurgey and NK Immunotherapy for Recurrent Cervical Cancer

Start date: July 1, 2016
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of this study is the safety and efficacy of cryosurgery plus NK immunotherapy to recurrent cervical cancer.

NCT ID: NCT02837926 Completed - Cervical Cancer Clinical Trials

Comparing Health Services Interventions for the Prevention of HPV-related Cancer

CoheaHr-WP4
Start date: May 2016
Phase: Phase 4
Study type: Interventional

The study aims to identify global and local determinants of HPV vaccine acceptability, HPV vaccine uptake and compliance as well as identify logistics and programmatic issues in each country to offer the HPV vaccine, as a potential cervical cancer prevention strategy, to mid-aged women attending screening.

NCT ID: NCT02825355 Completed - Clinical trials for Uterine Cervical Neoplasms

Sentinel Node Mapping in Women With Cervical and Endometrial Cancer

SENTIREC I
Start date: February 27, 2017
Phase:
Study type: Observational [Patient Registry]

This study aims to evaluate the effect of SLN mapping on the incidence and severity of lymphedema in women with early stage cervical and endometrial cancer.