Clinical Trials Logo

Uterine Cervical Dysplasia clinical trials

View clinical trials related to Uterine Cervical Dysplasia.

Filter by:
  • Not yet recruiting  
  • « Prev · Page 2

NCT ID: NCT04191603 Not yet recruiting - Cervical Dysplasia Clinical Trials

TWO DİFFERENT ELECTROSURGERY DEVICES AS MONOPOLAR HOOC AND PLASMAKINETIC BIPOLAR SPATULA EFFECTIVENESS DURING COLPOTOMY

Start date: October 30, 2020
Phase: N/A
Study type: Interventional

WE DECIDED TO COMPARE TWO DIFFERENT ELECTROSURGERY DEVİCES TO PROVIDE COLPOTOMY. ONE OF THEM İS MONOPOLAR HOOC, THE OTHER DEVİCE İS PLASMAKİNETİC BİPOLAR SPATULA. WE WİLL RANDOMİSE PATİENTS FİRSTLY THEN COMPARE THE RESULTS SUCH, VAGİNAL DEHİSSENS, COLPOTOMY DURATİON, AMOUNT OF MIST DURING COLPOTOMY, AMOUNT OF BLEEDİNG.

NCT ID: NCT03975127 Not yet recruiting - Cervical Carcinoma Clinical Trials

Cervical Cytology - Do SMS Reminders Increase Participation in the Cervical Screening Programme?

Start date: December 1, 2019
Phase: N/A
Study type: Interventional

This study will pilot production and evaluate the use of reminder information in women invited for cervical screening for the first time within the GGC eligible population for cervical screening. Women aged under 30 years will be identified to receive an SMS text message following their cervical screening invitation using information from the CHI Broadcast.

NCT ID: NCT03813576 Not yet recruiting - Cervical Cancer Clinical Trials

Acceptability and Efficacy of Self-sampling for Cervical Cancer Screening: A Pilot Study

Start date: March 2019
Phase: N/A
Study type: Interventional

In Singapore, the current cervical cancer screening uptake among women in Singapore has remained at low 50% since its introduction in 2004. It has been widely reported that under-screened women have the highest risk of cervical cancer. Self-sampling HPV DNA screening may be a solution to the low uptake rates of local women, particularly among the under-screened population in Singapore. Self-sampling comprises women using a swab to obtain samples from their vagina. In this study, we are comparing the sensitivity of detecting HPV positive women using HPV DNA test with self-sampling using flocked swab with the current physician sampling method. We also aim to determine acceptability of self-sampling HPV DNA test using flocked swab in cervical cancer screening. Designed as a feasibility study, it will comprise a prospective study of 300 women attending clinics in National University Hospital (NUH) and National Cancer Institute Singapore (NCIS).

NCT ID: NCT02955667 Not yet recruiting - Cervical Cancer Clinical Trials

The Application of Invivo Microscopy Imaging in the Early Diagnosis of Cervical Cancer

Start date: December 2016
Phase: N/A
Study type: Interventional

This study intends to carry out a prospective, randomized controlled trial to research and development a new invivo microscopy based on the technology which is combined with high-definition microscopy and colposcopy,so as to diagnose cervical lesion directly and non-invasively by observing cervical tissues and cells, which makes it possible to diagnose cervical cancer without wounds.

NCT ID: NCT02406391 Not yet recruiting - Cervical Cancer Clinical Trials

Adherence to Preventive Care for Cervical Cancer

Adh-NYC-EP
Start date: April 2015
Phase: N/A
Study type: Observational

In the United States, the highest incidence of cervical cancer occurs in inner city urban centers, rural areas, the deep South, Appalachia and the U.S.-Mexico border. The goal of this study is to study predictors of adherence among patients seeking care at an inner city medical center in New York City and the U.S. Mexico border for cervical cancer prevention, namely, Pap smears and colposcopy exams.