49 results
To investigate whether it is possible to manipulate perfusion in type 3 fibroids with MR-HIFU.
Primary Objective 1:Verfiy that energy can be transmitted from an external unit to the NSM AHLeveeS System, through a wireless connection, resulting in stimulation of the S3 sacral nerve.Primary Objective 2:Confirm that the NSM AHLeveeS System can…
To evaluate the subjective and objective cure after surgical re-intervention due to mesh complications in our clinical setting in order to optimize therapy.
To determine which advanced image enhanced modality is the most feasible for the detection of endometriosis lesions, with respect to the specificity and sensitivity of the investigated modalities. To determine which imaging modality reveals more…
The main objectives of this study are to evaluate the performance and ease of use of the Follow me mode of the AutoLap system during general and gynecological laparoscopic procedures.Study Procedures: No. & type. A total of 35 laparoscopic…
In this controlled (studygroups from P05-095 will serve as controls) observational study, the effects of radiation therapy after nerve-sparing radical hysterectomy for early stage cervical cancer on sexual function, bladder and bowel function is…
The primary objective is to assess the differences in mobility of pelvic organs between three commonly performed treatment options for uterine descent (vaginal hysterectomy, vaginal sacrospinous hysteropexy and laparoscopic sacrohysteropexy). The…
The primary objective of this clinical trial is to evaluate the safety and effectiveness of the AltaSeal® implants in providing bilateral mechanical occlusion of the fallopian tubes and in preventing pregnancy.Additional objectives are as follows:*…
Observational multicenter trialThe following research questions (Q) will be addressed in patients (and partners) (Q1) whether sexual problems as reported by female cancer survivors are personally distressing and if so, ( Q2) what are possible…
The purpose of this study is to demonstrate that the use of the Vapor System is safe and effective. It will be tested in patients who were already planned to undergo a hysterectomy and the device thus has no therapeutic purpose in this particular…
The primary aim of this study is to gain more insight on the impact of reconstructive surgery on circumcised women (type I, 2 & 3). This study may also used for theorizing about plastic surgery on women who are circumcised.
The primary aim of this research project is to investigate the prevalence and bother of OAB before and after POP repair surgery and to determine changes in bladder function after surgery. Secondary aim is to identify predictors of persistence,…
1. to measure anatomical outcome after vaginal repair with mesh (Prolift technique) and compare with pre-operative scorings, using POP-Q test.2. to estimate quality of life, sexual functioning, urogenital en defecatory symptoms after vaginal repair…
1. To assess the effects of prolapse surgery on vaginal nerve density2. To measure the association between changes in vaginal nerve density and changes in pelvic floor function
Objectives: The purpose of this study is to establish the safety of the product.This study is designed to evaluate the safety of the device in protecting the anastomotic junction created during a stoma reversal procedure. The objectives of this…
1. To assess anatomical outcome before and after sacrospinous hysteropexy by a POP-Q and to compare with anatomical situation before surgery.2. To assess urogenital and defecatory symptoms, sexual disfunction and quality of life after sacrospinous…
The primary objective of this study is to evaluate the anatomical success of the GYNECARE PROLIFT + M* system in women with symptomatic ICS POP-Q Stage III or IV, requiring surgical correction of pelvic organ prolapse (POP). Secondary objectives…
The primary objective of this study is to evaluate the technical success, feasibility and safety of hysteroscopic US guided cryomyolysis procedure.
The primary objective of this study is to evaluate the safety and effectiveness of Doppler guided Uterine Artery Occlusion (D-UAO) as treatment for the reduction of fibroid-associated symptoms.
To test an intra-operative fluorescent camera system with a fluorescent optical agent in detection of the sentinel lymph node. This will be compared to the standard method with radiocolloid and patent blue.