341 results
This study has been transitioned to CTIS with ID 2024-518101-18-02 check the CTIS register for the current data. The main objective of this project is to associate the gut microbial community with treatment efficacy (i.e., relieve in symptoms and…
Primary objectives are to investigate (1) the prevalence and nature of sexual dysfunctions in patients meeting the criteria for PTSD or OCD, and; (2) whether sexual dysfunctions decreases after the guideline treatment aimed at PTSD or OCD. Secondary…
The primary objective of this study is to assess the potential of quantitative MRI parameters to predict nodal disease stage of prostate cancer by correlating quantitative MRI measurements of the local prostate to the presence of metastases as seen…
Primary objectiveThe key objective is to examine the anti-body immune response to SARS-CoV-2 vaccination in shift workers, compared to dayworkers, Secondary objectives:• To tinvestigate whether sleep duration, independent of circadian misalignment,…
The primary objective is to clarify the frequency of t-BPPV in patients after mild TBI. Secondary objectives are: assessment of the symptoms of t-BPPV and the treatment success of t-BPPV.
Primary Objective:Our main objective is to analyse if the microbiota composition of the affected skin is different from the non-affected skin in XRI and ARCI. Secondary Objectives:(1) To investigate the composition of the skin microbiota of patients…
Primary Objective: to evaluate clinical efficacy of domatinostat in combination with avelumab in treatment-naïve metastatic or distally recurrent MCC patients as determined by the Objective Response Rate (ORR) according to Response Evaluation…
Primary Objective: To investigate in surgical ward patients whether the use of wireless continuous vital signs monitoring will reduce total length of hospital stay.
The primary objective is to study the association between baseline (including genetic), and repeatedly measured blood biomarkers (including metabolomics and proteomics), and the incidence of cardiovascular disease. Secondary objectives are related…
The primary objective of our pilot study is to assess trial feasibility. Our secondary pilot objectives are to collect data on patient experience of healthcare, patient engagement, cost-effectiveness, and other data that might inform the design of a…
The aim of this pilot study is to determine the diagnostic value of exhaled breath analysis by eNose technology for endometriosis patients: does it detect endometriosis?
Primary objective: To determine the seroprevalence of WNV and USUV antibodies in serum samples from bird ringers in The Netherlands.
The specific trial aim is to establish whether the use of a high, dynamic 8-12 cmH2O PEEP level strategy to support the lung during stabilisation at birth, compared with a static 5-6 cmH2O PEEP level strategy, increases the rate of survival without…
The primary objective of the MIDDEL trial is to provide high-quality evidence of the comparative effectiveness of group music therapy, recreational choir singing, group music therapy plus recreational choir singing, or standard care alone, for…
To assess the potential of AT1R and ETAR antibodies to serve as a biomarkers for clinical deterioration in COVID-19.
The main objective of this study is to perform a quality assessment on several new techniques, used in the laboratory of Translational Cancer Genomics and Proteomics
2.1 Primary The primary objective of the study is to evaluate the efficacy of troriluzole as adjunctive therapy compared to placebo in subjects with OCD who have had an inadequate response to their current OCD treatment based on the change in their…
To assess the performance of the EndoRotor, as compared to conventional endoscopic techniques, for direct endoscopic necrosectomy (DEN) of walled off necrosis (WON)
To prospectively assess the potential effect of repeated exposure to either a linear or amacrocyclic gadolinium-based contrast agent (GBCA) on change from baseline to Year 5 inmotor and cognitive function among neurologically normal adults in…
This study has been transitioned to CTIS with ID 2024-512558-40-00 check the CTIS register for the current data. Primary• Evaluate the efficacy of 8 weeks of treatment with VE202 in terms of endoscopic response at Day 56 • Evaluate the safety of…