50 results
Primary objectives: To compare the dose volume histograms (DVHs) of the planning target volume (PTV) in prone and supine position, with 3D conformal and intensity-modulated radiotherapy (IMRT) planning in patients who receive pelvic irradiation To…
To compare sexual functioning and complaints concerning micturation and defecation in women after abdominal or vaginal trachelectomy for early stage cervical cancer.
To test a near-infrared fluorescence camerasystem in order to detect folate-FITC in tumour tissue in women with ovarian cancer who undergo cytoreductive surgery.
To determine the incidence and grade of venous emboli and/or paradoxical gas emboli during hysteroscopy surgery using TOE. In addition, a comparison will be made using either bipolar or monopolar diathermia. Knowing the incidence and severity of…
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.
1. Compare generic and pelvic-floor-specific QOL in patients who have been treated or gynaecologic cancer to that of patients without cancer attending a gynaecologist for pelvic floor symptoms.2. Examine how many and which patients receive or have…
SCAR study
Sonohysterographic evaluation of caesarean scar defects and determination of risk factors
Determination of the incidence of a scar defect .Determination of riskfactors for develpment of scar defects
This study will investigate a comparison group of women treated with a conventional (non-nerve sparing) RHL for cervical cancer (CC) at the Academic Medical Centre (AMC). Together with the data collected of women treated with a nerve sparing radical…
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/…
1. To assess the feasibility of SLN identification in endometrial cancer.2. To examine in how many cases SLN biopsy provides results that will tailor adjuvant treatment3. To investigate if SLN biopsy in women with low- and intermediate-risk…
OBJECTIVE: through MRI research, we want to map the pelvic floor structures that are involved in holding a pessary in place
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.
The primary objective of this study is to develop an diagnostic algorithm using ct-DNA, and TEPs as liquid biomarkers in combination with the existing ultrasound models (RMI and IOTA-models) and biomarkers (CA125 and HE4) to differentiate between…
Primary objective: To identify those groups of pregnant patients, planned to undergo cesarean delivery, who are at risk to develop severe hypotension (defined as a decrease of at least15% from the baseline tension) based on their preoperative volume…
The objective of the present study is to evaluate the safety of Womed Leaf after hysteroscopic myomectomy and its potential efficacy in preventing IUA at second look hysteroscopy.
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.
Objective:The life-time risk for POP surgery is 20%, and 30% of these women will need surgery because of a recurrence. VaginalPOP surgery (VH, SSH and MM) is the first choice surgical treatment. The numbers of uterus sparing operations (SSH andMM)…
The primary objective of this study is to assess the feasibility of EM-navigation for gynaecological brachytherapy catheter placement.
This study has been transitioned to CTIS with ID 2024-512862-32-00 check the CTIS register for the current data. The primary objectives of this trial are to study clinical efficacy and immune activation of neoadjuvant PD-1 blockade in VSCC.