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Sexual function in women with Polycystic Ovary Syndrome

to assess general sexual functioning, genital sexual responsiveness, subjective sexual responsiveness and affect in women with PCOS , and to make a comparison of these results with the results of an age matched healthy control group of women.…

Treatment Response in Non-Affective Psychosis.

1) To compare between treatment responders, treatment non-responders, and healthy controls: sDSC and GABA in the ACC;2) To assess, in psychotic patients and healthy controls, whether AEA and 2-AG plasma levels are associated with sDSC, and…

DISCOvERIE: Development, dIagnosis, and prevention of gender-related Somatic and mental COmorbitiEs in iRritable bowel syndrome In Europe

To provide an extensive clinical and psychosocial characterization of IBS patients with and without psychological and/or physical comorbidities, as well as of disease-controls without IBS, but with psychological and/or physical disease, and a…

Immunity against SARS-CoV-2 Omicron variant

The key objective of the study is to characterize the immune response against SARS-CoV-2 omicron variant. Secondary objectives:1. Does the clinical course of disease correlate to viral loads and the immune response?2. How is the CT value of the PCR…

*The Experience Sampling Method (ESM):
a real-time Patient-Reported Outcome Measure for symptom assessment in patients with overactive bladder syndrome.*

This project will be subdivided into three sections:Part I. Comparison of the ESM vs. SR-BDs and other retrospective questionnaires in the assessment of urological complaints in OAB such as urgency. Part II. Validation of new patient-reported…

Fabry Exercise Intolerance STudy

Primary Objective(s):1. To study the presence and extend of exercise intolerance in male, female FD patients with classical FD and men with non-classical FD, in different stages of the disease.2. To determine the aetiology of exercise intolerance in…

*A prospective randomized multicenter study to demonstrate the superiority of the Barricaid® to discectomy for primary lumbar disc herniation*: Extended Follow-Up of the Barricaid® Annular Closure Device (ACD) Randomized Control Trial (RCT) Postmarket Cohort for Lumbar Disc Herniation and Interaction with Other Risk Factors

The purpose of this post-approval protocol amendment is to extend the follow-up of subjects who were originally enrolled in theRCT, EUBARD-CP_001 protocol. This study extension will examine the long-term survivorship of the Barricaid® ACD when…

A randomized controlled trial on the visual function after bilateral implantation of two novel Extended Depth-of-Focus intraocular lenses.

The primary objective of this study is to compare the binocular uncorrected intermediate visual acuity (UIVA) at 66 cm under photopic conditions 3 months postoperatively, in a series of patients bilaterally implanted with the Acunex® Vario IOL…