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NCT ID: NCT03039387 Recruiting - Major Depression Clinical Trials

Effects of tDCS on Cognitive Control and Emotion Regulation in Depressed Patients

Start date: September 2016
Phase: N/A
Study type: Interventional

Deficient cognitive control (CC) and the use of dysfunctional emotion regulation strategies (ERS) are both central characteristics of major depression. Both are associated with reduced activity of the dorsolateral prefrontal cortex (dlPFC). Transcranial direct current stimulation (tDCS) is a safe, simple and effective non-invasive method to modulate the cortical excitability. The goal of this randomized, sham-controlled, double blind clinical trial is to examine the effect of transcranial direct current stimulation (tDCS) on the CC and ERS in depressed patients compared to healthy subjects. Overall, the study will include 44 participants (22 depressed Patients and 22 healthy subjects). Each participant will complete a CC task while receiving sham tDCS in one session and anodal tDCS in the other session (counterbalanced). Afterwards the ERS 'rumination' will be measured during a resting phase by means of a questionnaire and psychophysiological measures (heart rate variability). The investigators hypothesize (a) an amelioration of CC by anodal tDCS and (b) a reduced use of the dysfunctional emotion regulation strategy 'rumination' after anodal tDCS. Overall this experiment will provide new and reliable data for the development of new treatment methods.

NCT ID: NCT03038464 Recruiting - Clinical trials for Diagnosis Prosthetic Joint Infection

Synovial Aspiration and Serological Testing in Two-stage Revision Arthroplasty of Prosthetic Joint Infection

SyPJI
Start date: November 1, 2016
Phase: N/A
Study type: Observational

The two-stage protocol is gold standard in terms of infection control treating prosthetic joint infections of total hip and total knee arthroplasty. The antibiotic pause for diagnostic reasons before reconstruction (stage two) is discussed concerning persistence of infection and development of resistant bacterial strains. Serological markers and synovial analysis are common use to exclude persistence of infection. The investigators therefore asked 1) is the serological testing of c-reactive protein and leukocytes a valuable tool to predict a persistence of infection and 2) what is the role of synovial aspiration of PMMA Spacers on hip and knee joints.

NCT ID: NCT03037398 Recruiting - Parkinson Disease Clinical Trials

Closed Loop Programming Evaluation Using External Responses for Deep Brain Stimulation

CLOVER
Start date: January 11, 2017
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the performance of novel DBS programming methods compared to traditional programming methods.

NCT ID: NCT03036969 Recruiting - Clinical trials for Non-urgent Emergencies

EPICS-8: Reasons for Emergency Department Utilization by Patients With Non-urgent Conditions

EPICS-8
Start date: May 2016
Phase:
Study type: Observational

EPICS-8: Reasons for Emergency Department utilization by patients with non-urgent conditions: Emergency Departments (EDs) are an important interface between primary and secondary health care sectors in Germany. The number of outpatient visits in the ED´s is still increasing. The reasons for ED utilization by patients with non-urgent conditions are nearly unknown in Germany and will be investigated in this project.

NCT ID: NCT03035669 Recruiting - Clinical trials for Stress, Psychological

Effects of Mindfulness Training on Emotion Regulation and Social Cognition.

MFN&SOCCOG
Start date: November 2016
Phase: N/A
Study type: Interventional

The present study will investigate the effects of a mindfulness training on emotion regulation and social cognition, using several psychological, behavioral, psychophysiological and neuroimaging methods.

NCT ID: NCT03032562 Recruiting - Clinical trials for Respiratory Muscle Paralysis

Respiratory Muscle Strength and Function in Neuromuscular Disorders and Chronic Obstructive Pulmonary Disease

Start date: December 1, 2016
Phase: N/A
Study type: Observational

Using an extensive set of both volitional and non-volitional tests of respiratory muscle function and strength it is the aim of this study to - identify disease-specific patterns of respiratory muscle impairment in different NMD and COPD - establish which set of tests is predictive of sleep-disordered breathing or daytime hypercapnia in patients with NMD or COPD, respectively. - to investigate the decline of respiratory muscle function in patients with progressive NMD and COPD along with sleep studies and capnography

NCT ID: NCT03027596 Recruiting - Burns Clinical Trials

Remote Ischemic Conditioning to Reduce Burn Wound Progression

RIC in burns
Start date: January 2017
Phase: N/A
Study type: Interventional

Burned skin areas, which were initially vital, can be irreversibly damaged by wound progression. The aim of the present study is to evaluate the feasibility of ischemic conditioning to reduce secondary wound progression.

NCT ID: NCT03022851 Recruiting - Clinical trials for Pulmonary Hypertension

The Prophet Trial -Pilot Study to Assess Safety and Efficacy of a Novel Atrial Flow Regulator (AFR) in Patients With Pulmonary Hypertension

AFR-Prophet
Start date: July 19, 2017
Phase: N/A
Study type: Interventional

This study aims to investigate safety and efficacy of Occlutech® AFR device in patients with severe pulmonary hypertension (PH).

NCT ID: NCT03022721 Recruiting - Clinical trials for Diabetes Complications

Heidelberg Study on Diabetes and Complications

HEIST-DiC
Start date: September 2016
Phase: N/A
Study type: Observational

The prospective observational study entitled "Heidelberg Study on Diabetes and Complications" is designed to Monitor the presence and development of diabetic complications in type 1 and type 2 diabetic patients, as well as pre-diabetics. Mail Goal is to detect new metabolic mechanisms or new risk factors for the development of diabetic complications in order to identify risk-subgroups. Non-diabetic controls will be enrolled for reference and comparison.

NCT ID: NCT03020043 Recruiting - Clinical trials for Chronic Heart Failure

Evaluation of Longterm Outcome of New York Heart Association Class III Heart Failure Patients Receiving Telemonitoring Using a Pulmonary Artery Pressure Sensor System (CardioMEMS)

Start date: August 2016
Phase:
Study type: Observational [Patient Registry]

Invasive hemodynamic monitoring in advanced heart failure patients is a relative new option. In order to investigate the impact of remote telemonitoring of pulmonary artery pressures on mortality and morbidity in a routine clinical setting in Germany, the investigators initiated this multicenbtric registry.