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NCT ID: NCT04042792 Completed - Rheumatic Diseases Clinical Trials

Characterization of Adalimumab Concentrations in Pediatric Patients With Inflammatory Rheumatic Disease With and Without Methotrexate

ADA in PiRD
Start date: September 26, 2019
Phase:
Study type: Observational

This study is to assess standardized Adalimumab (ADA) concentrations in Pediatric inflammatory rheumatic diseases (PiRD) patients treated with ADA for ≥ 12 weeks with and without concomitant methotrexate (MTX) therapy and to assess peak and trough ADA concentrations in ADA naïve patients after first ADA administration with and without MTX (pre-phase).

NCT ID: NCT04042779 Completed - Working Memory Clinical Trials

Development of a Model-based Working Memory Training and Investigation of Its Comparative Efficacy

sMarT
Start date: July 2, 2019
Phase: N/A
Study type: Interventional

This study is to investigate the efficacy of model-based Working Memory (WM) training using an appropriate control condition. The interventions are a model-based, a single-task and a multiple-task training on WM in order to compare the efficacies of these different training approaches for WM. A sham intervention acts as active control group. Each intervention will be presented on a tablet device.

NCT ID: NCT04036123 Completed - Clinical trials for Lower Urinary Tract Dysfunction

Urodynamic Assessment of the Lower Urinary Tract: Water vs. Air - Synchrony

Start date: October 1, 2019
Phase: N/A
Study type: Interventional

Comparison of water-perfused (WP) and air-charged (AC) catheters for invasive urodynamic investigation (UDI) regarding consistency, features and artifacts.

NCT ID: NCT04035993 Completed - Diabetes Clinical Trials

The HEADWIND-Study

HEADWIND
Start date: October 7, 2019
Phase: N/A
Study type: Interventional

To analyse driving behavior of individuals with type 1 diabetes in eu- and progressive hypoglycaemia using a validated research driving simulator. Based on the driving variables provided by the simulator the investigators aim at establishing algorithms capable of discriminating eu- and hypoglycemic driving patterns using machine learning neural networks (deep machine learning classifiers).

NCT ID: NCT04035031 Completed - Clinical trials for Diabetes Mellitus, Type 1

Effects of Dapagliflozin on Hormonal Glucose Homeostasis in Type 1 Diabetes

Start date: January 9, 2020
Phase: Phase 3
Study type: Interventional

Inhibitors of sodium-dependent glucose-transporter 2 (including dapagliflozin) represent intensively investigated drugs in the field of diabetes. SGLT-2 inhibition limits glucose reabsorption in renal tubular cells, hereby increasing the amount of glucose excreted via urine in the hyperglycemic state. Its mechanisms of action are independent of insulin, the indispensable standard of care in Type 1 Diabetes (T1D). Several international diabetes experts highlighted the need for adjunct therapies in T1D. Subcutaneous application of insulin is non-physiological. Most significant, subcutaneous insulin substitution does not address the bi-hormonal character of T1D. The loss of pancreatic beta cells and subsequent endogenous insulin production uncouples alpha cell derived glucagon secretion from its paracrine suppressor. Consequently, excess glucagon concentrations occur in the fasting and the postprandial state, which promotes hyperglycemia, requires higher doses of subcutaneous insulin, and promotes glycaemic variability. Recent studies on SGLT-2 inhibition in T1D showed better glycemic control compared to placebo, whereas a higher risk for the development of diabetic ketoacidosis was observed. Knowledge about the underlying mechanisms is scarce. Studies showed that SGLT-inhibition increased Glucagon-like-peptide 1 (GLP-1) in T1D, an incretin hormone capable of suppressing glucagon. On the other side, total concentrations of ketone bodies were higher following SGLT-2 inhibition, irrespective of ongoing subcutaneous or intravenous insulin substitution. The present study aims to investigate the effect of SGLT-2 inhibitor dapagliflozin on hormonal regulators of glucose homeostasis and ketogenesis in T1D. The primary endpoint is the difference of GLP-1 during oral glucose tolerance test clamps (OGGTc). Secondary endpoints comprise total ketone body concentrations, free fatty acids, glucagon, and somatostatin during OGTTc and hyperinsulinemic, euglycemic clamps (HEC) following dapagliflozin and placebo. The study recruits male and female patients with T1DM in a randomized, open label, cross-over intervention study.

NCT ID: NCT04033783 Completed - COPD Clinical Trials

Impact of Walking Behind the COPD Patient on 6MWD

Start date: September 18, 2019
Phase: N/A
Study type: Interventional

The six-minute walk test (6MWT) is a well established field exercise test to assess the functional exercise capacity in chronic obstructive pulmonary disease (COPD). The objective of this study is to assess the impact of walking behind the patient on 6MWT distance in patients with COPD.

NCT ID: NCT04033770 Completed - Clinical trials for Lower Urinary Tract Dysfunction

Urodynamic Assessment of the Lower Urinary Tract: Water vs. Air

Start date: February 1, 2021
Phase: N/A
Study type: Interventional

Comparison of water-perfused (WP) and air-charged (AC) catheters for invasive urodynamic investigation (UDI) regarding consistency, features and artifacts.

NCT ID: NCT04033367 Completed - Atopic Dermatitis Clinical Trials

SAR231893-LPS15497- "Dupilumab Effect on Sleep in AD Patients"

Start date: August 22, 2019
Phase: Phase 4
Study type: Interventional

Primary Objective: To evaluate the effect of dupilumab on sleep quality in adult participants with moderate to severe atopic dermatitis (AD). Secondary Objectives: To evaluate the effect of dupilumab on objective and subjective quantitative sleep parameters, AD related outcomes, and daytime consequences of sleep deprivation. To continue to assess the safety and tolerability throughout the study.

NCT ID: NCT04032314 Completed - Clinical trials for Spinal Cord Injuries

Lower Extremity Outcome Measures in SCI

Start date: December 1, 2018
Phase:
Study type: Observational

Lower extremity (LE) function of patients with a spinal cord injury (SCI) will be assessed in an observational project with a cross-sectional and a longitudinal study design. The main goal is to identify kinematic and kinetic parameters to precisely characterize LE function and in parallel the impairment and limitation in SCI patients throughout rehabilitation in acute patients and in chronic patients to define LE function and LE recovery.

NCT ID: NCT04029142 Completed - Hemoglobinopathies Clinical Trials

Screening for Hemoglobinopathies in Pregnant Women

Start date: July 3, 2019
Phase:
Study type: Observational

This prospective monocentric study project is to identify hemoglobinopathies in pregnant women in order to optimize antenatal care and to investigate the prevalence of hemoglobinopathies in pregnant women in Switzerland.