25 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.
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 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…
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 compare sexual functioning and complaints concerning micturation and defecation in women after abdominal or vaginal trachelectomy for early stage cervical cancer.
The primary objective is to gain experience with primary radiochemotherapy and to determine the locoregional response rate at 12 weeks after radiochemotherapy and after groin dissection for cN1,2 patients.
The objective of the study is to evaluate the subjective and objective effectivity and safety of the laparoscopic sacrocolpopexy of 189 patients who underwent this procedure in the period August 2004 - December 2014 in the Diakonessenhuis Utrecht/…
To establish the safety and effectiveness of the Sonata System in the treatment of symptomatic uterine fibroids.
To evaluate the pain reducing effect of MCRRF therapy in women with persisting perineal pain after episiotomy using Visual Analogue Scale (VAS) scores.
To evaluate the feasibility of MCRRF therapy in women with persisting perineal pain after episiotomy. Collection of pilot data is essential in the preparation of a larger randomized-controlled trial that investigates the efficacy of MCRRF therapy.