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NCT ID: NCT02689700 Recruiting - Clinical trials for Materno-fetal Transfer of Anti-VZV-IgG

Diaplacental Transfer of Anti-HCMV- and Anti-VZV-immunoglobulin G (IgG) -Antibodies at Premature and Mature Newborns

MoChi-HCMV
Start date: July 2013
Phase: N/A
Study type: Observational

The aim of the study is to determine the total concentration of HCMV- and VZV-specific IgG-antibodies and the total concentration of neutralizing antibodies against HCMV in neonatal bloodstream depending on gestational age at birth.

NCT ID: NCT02687568 Recruiting - Clinical trials for Electroencephalography

Values of Enhanced Monitoring by EEG Recording (Narcotrend) for Sedation in Colonoscopy

Start date: May 2014
Phase: N/A
Study type: Observational

Endoscopic examinations and particularly long-lasting interventions can be uncomfortable for patients. Pain and vasovagal reactions are common. Therefore, the implementation is generally recommended under sedation and also carried out in practice here. The vital signs monitoring to avoid complications is dictated by current national guidelines. Necessary measures of monitoring include pulse oximetry and blood pressure measurements. In patients with severe heart disease an ECG recording should be used additionally. Moreover, the guidelines require that the sedation is clinically monitored continuously to avoid an unwanted anesthetic stage. Such evaluation, however, is often difficult under clinical conditions and even counterproductive, since a constant response and tactile stimulation of the patient (to check clinically the depth level of sedation ), interrupts endoscopic complex intervention. However, clinical most relevant aspect is the avoidance of unrecognized transition of patients from the stage of deep sedation in an anesthetic stage. Current recommendations do not take into account new study results from a gender perspective, which showed that women and men need a different wake-up time using the EEG derivation means by using the Narcotrend after total intravenous anesthesia, which may be due to different total doses of sedatives needed. However, the research group has been demonstrated in a previous study that most likely caused by the use of EEG monitoring (Narcotrend) an effective adaptation of sedation, in particular a more rapid recovery time by a lower dose of the administered sedative for a continuous sedation stage D0-D2 endoscopic retrograde cholangiopancreatography-(ERCP). In the presented study the investigators evaluate the extent of gender differences in the wake-up time after sedation with propofol during colonoscopy when using EEG monitoring.

NCT ID: NCT02686554 Recruiting - Alzheimer Disease Clinical Trials

Identification of Proteostasis-related Biomarkers in Alzheimer´s Dementia

Start date: January 2016
Phase:
Study type: Observational

At the time of biomarker-substantiated diagnosis for a given AD patient it remains unclear to what extent the disease will devastate cognitive abilities within the next years. This is not only unsatisfying for the patient and the attending physician but also a major problem in the context of clinical trials that aim to establish new therapeutic agents. In clinical trials it is critically important to foresee as precisely as possible the course of the disease. The overall aim of the subproject is to identify a panel of CSF biomarkers to further improve specificity of diagnosis ("disease markers"), to measure disease activity and to predict AD progression ("stage and progression markers").

NCT ID: NCT02686229 Recruiting - Glioma Clinical Trials

Registry Study on Epidemiological and Biological Disease Profile as Well as Clinical Outcome in Patients With Low Grade Gliomas

LoG-Glio
Start date: November 15, 2015
Phase:
Study type: Observational [Patient Registry]

The LoG-Glio-Registry is based on a network of german hospitals gathering radiological, clinical, epidemiological and molecular data on all patients diagnosed with a low grade glioma.

NCT ID: NCT02686125 Recruiting - Dystonia Clinical Trials

Vercise™ DBS Dystonia Prospective Study

Start date: March 7, 2016
Phase:
Study type: Observational [Patient Registry]

To compile characteristics of real-world outcomes of Boston Scientific Corporation's commercially approved VerciseTM Deep Brain Stimulation (DBS) Systems for the treatment of dystonia.

NCT ID: NCT02685605 Recruiting - Glioblastoma Clinical Trials

Intraoperative Radiotherapy in Newly Diagnosed Glioblastoma Multiforme

INTRAGO-II
Start date: December 9, 2016
Phase: Phase 3
Study type: Interventional

INTRAGO II resembles a multicentric, prospective, randomized, 2-arm, open-label clinical phase III trial which tests if the median progression-free survival (PFS) of patients with newly diagnosed glioblastoma multiforme (GBM) can be improved by the addition of intraoperative radiotherapy (IORT) to standard radiochemotherapy.

NCT ID: NCT02682550 Recruiting - Multiple Trauma Clinical Trials

Danger Response in Polytrauma Patients

NTF-PT
Start date: September 2014
Phase: N/A
Study type: Observational

The NTF_PT_2014 multicenter study aims to collect, store, and analyse plasma and serum from polytrauma-patients (injury severity score ≥25) and corresponding clinical data to address 1) how trauma modulates the release of danger molecules, inflammatory mediators, coagulation factors and novel biomarkers, 2) how the specific injury pattern affects the posttraumatic response and regenerative potential on an organ-, cell, and molecular level, and 3) how could a specific organ- and immune-monitoring predict the clinical outcome.

NCT ID: NCT02682537 Recruiting - Healthy Clinical Trials

IC-BASAROTs: New Practice Method for More Accurate Bed-side Assessment of Individual Energy Expenditure

Start date: March 2015
Phase:
Study type: Observational

Assessment of resting energy expenditure (REE) by indirect calorimetry (IC) in 1400 healthy individuals for arithmetical transformation into an bedside tool to estimate energy requirements in dietary practice (BASAROTs). A multinational, multicenter, prospective cross-sectional study.

NCT ID: NCT02681068 Recruiting - Clinical trials for Clostridium Infections

MicroTrans - A Multicenter Registry of Fecal Microbiota Transplantation

MicroTrans
Start date: January 2015
Phase: N/A
Study type: Observational

The registry collects cases of patients received fecal microbiota transplantation (FMT) due to Clostridium difficile associated diarrhea (CDAD). The main objective of this study is to analyze the safety and effectiveness of FMT. Furthermore, data analysis will be used to implement a standardization of FMT in German hospitals and improve patient outcome. Therefore, a detailed description of completions of FMT are documented on our web-based survey platform www.ClinicalSurveys.net.

NCT ID: NCT02676414 Recruiting - Clinical trials for Arterial Hypertension

Validation of a Hypertension Education Program

Start date: August 2015
Phase: N/A
Study type: Interventional

The primary purpose of this study is to assess the effect of participating in the interactive hypertension education program of the German Hypertension League (DHL©) "My blood pressure - OK!" on office systolic blood pressure.