430 results
Determining the feasibility of EVNS performed at home by the patient and/or caregiver, after instruction from the podiatrist.
Aim of the ACTOR project is to develop organoid models for anal SCC, both in the non-metastatic and in the metastatic setting to: 1) learn about the biology of disease by characterising the organoids and original tissue, circulating immune cells and…
This study aims to investigate proof of principle of utilizing nCLE during CBCT-NB navigation bronchoscopy. A confirmatory CBCT spin is considered the gold standard for tool-in-lesion but is associated with additional radiation exposure. We aim to…
With this study we want to test the user experience of the prototype app and to develop a method to identify subtypes of post-covid patients and link this to demografic, medical and sociopychological characteristics as predictors.
The objective of the study will be to analyse the diagnostic and prognostic value of circulating inflammatory and/or coagulation biomarkers in plasma, plasma Extracellular Vesicles (EV), and gene expression profiles of circulating cells for the…
1. To identify the perceived barriers and facilitators for initiating and maintaining a healthy lifestyle in people with both DM2 and a low SEP. 2. To co-create a digital, personalised CBT lifestyle tool together with end users (people with DM2) to…
The purpose of this clinical study is to collect safety and efficacy data of the VDyne System to support Conformitè Europëenne (CE) Mark of the VDyne System.
To develop, optimize and evaluate MRI sequences and technology.
The objective of this study is to evaluate the insulin delivery of the Medtronic Implantable Insulin Pump System (MIIPS 2020).
The primary objective:- To investigate the feasibility of capturing in-vivo cross section images of the bladder wall in bladder cancer patients with the OCT catheter.Secondary objectives:- To evaluate the duration of the OCT measurements. - To…
To demonstrate that in post-MI patients with symptomatic heart failure who receive optimal medical therapy (OMT) for this condition, and with reduced LVEF <=35%, OMT without implantable cardioverter defibrillator (ICD) implantation (index…
Primary objective of the study is to determine whether prolonged use of 96 hours leads to growth of microorganisms (type and numbers (CFU/ml)) in enteral tube feeding sets. Secondary objectives are the occurrence of gastrointestinal events/ new…
The primary objective of this study is to evaluate the efficacy of the AtMoves Knee System in the clinical diagnostic process of aseptic knee loosening in knee prostheses. This will be measured by the number of *failed outcomes* resulting from…
Evaluate the efficacy and safety of the Matrix Pro Applicator on Profound Matrix system in the treatment of facial, submental and neck laxity.
To Identify genetic variants and clinical phenotypes associated with risk of HS and to characterize the key cellular and molecular mechanisms and pathways involved in the pathogenesis of moderate-to-severe HS.
To evaluate the safety and performance, including clinical benefit, of the PRIMUS System for the treatment of Resistant Migraine.
rTMS is an intensive but effective treatment that could benefit from further optimization. Cognitive control training (CCT) engages the same underlying neural circuitry as rTMS and has been shown to improve therapeutic response (Koster et al., 2017…
To investigate whether personalized hemodynamic management targeting baseline cardiac index reduces the incidence of a composite outcome of acute kidney injury, acute myocardial injury, non-fatal cardiac arrest, severe infectious complications, and…
• To evaluate the response to an in vivo immune challenge (KLH) in RA patients in responders versus non-responders to MTX therapy.• To evaluate the immune status of RA patients before and after the start of MTX therapy using an ex vivo immune…
Primary Objective:The primary objective of this trial is to test whether lymphatic surgery provides better QoL (assessed with the Lymph-ICF-UL, upper limb, questionnaire) 15 months after randomization (and therefore about one year after surgery)…