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Benign Hysterectomy clinical trials

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NCT ID: NCT05255120 Recruiting - Clinical trials for Postoperative Recovery

Hysterectomy - A Regional Intervention Study

HYSTERI
Start date: September 4, 2020
Phase: N/A
Study type: Interventional

Approximately 4,000 procedures with hysterectomy for benign indication are performed annually in Sweden. There are large differences in preoperative information, planning of surgery and surgical technique. A structured approach including the use of mobile phone technology can possibly improve patient information and patient involvement. Our purpose is to to evaluate whether systematic preoperative preparation improves the outcome of elective hysterectomy on benign indication.

NCT ID: NCT02859272 Active, not recruiting - Benign Hysterectomy Clinical Trials

Vaginal Vault Suspension During Benign Hysterectomy. A Questionnaire and Register-based Study.

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

Female pelvic organ prolapse (POP) is characterized by lack of vaginal support which enables pelvic organs to bulge into the vaginal walls and sometimes protrude through the genital hiatus. POP is more frequent among women who had their uterus removed. We would like to investigate whether suspension of the top of the vagina during remowal of the uterus prevents subsequent POP. The purpose of the PhD project is therefore to describe validity, terminology, and operative performance of used suspension methods during benign hysterectomy in Denmark. Further, to investigate these suspension methods' possible association with pain, life quality, sexuality, pessary use, and POP .

NCT ID: NCT02163239 Terminated - Cholecystectomy Clinical Trials

Post Market Study for FloShield 10mm Reusable Cannula and Blunt Obturator and Robotic FloShield

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

This study evaluates the use of the FloShield System with the FloShield 10mm reusable Cannula and Oburator during standard robotic laparoscopic single-site surgery. The study will evaluate the compatibility of the FloShield 10mm Cannula and Oburator with the daVinci® Robotic Surgical System during single-site laparoscopic surgery.