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NCT ID: NCT02059538 Recruiting - Clinical trials for Cardiometabolic Disease

Metagenomics and Integrative Systems Medicine of Cardiometabolic Diseases

METACARDIS
Start date: June 2013
Phase: N/A
Study type: Interventional

Supported by state-of-the-art systems medicine competences including integrative computational and functional genomics, the overarching goal of the trial is to investigate the impact of qualitative and quantitative changes in the gut microbiota on the pathogenesis of cardiometabolic diseases (CMDs) and their associated co-morbidities. A major objective will be to translate the clinical and fundamental based discoveries into new diagnosis and preventive actions paving the way to novel modes of treatment in the successive stages of CMD progression.

NCT ID: NCT02054494 Recruiting - HIV Clinical Trials

T1 Mapping in HIV Patients With High and Low CD4+ Cell Counts

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

HIV-infection is associated with an increased risk for cardiovascular disease. Especially patients with low CD4+ counts have a higher incidence of structural heart disease. Myocardial T1 relaxation time, as well as T1-derived extracellular volume fraction are relatively new methods for non-invasive myocardial tissue characterization, including diffuse myocardial fibrosis. In our study HIV-patients with high and low CD4+ counts are examined on a 3T MRI scanner (Ingenia 3T, Philips Medical, Best, Netherlands). Scanning protocol includes common SSFP sequences, STIR imaging and LGE [Late gadolinium enhancement]. All HIV patients are treated in the HIV outpatient clinic of the hospital's Internal Medicine department and have an unremarkable history of cardiac disease. Patients are recruited from all over Germany. In order to obtain reference values, a subgroup of healthy, age-matched controls is included in this study. Aim of this study is to show differences in T1- and ECV-values in the investigated subgroups. In addition, we also want to create cut-off values for healthy and affected myocardium in asymptomatic HIV-infected patients. This study could show whether myocardial T1 mapping is a potential screening parameter for beginning heart disease as part of an HIV-infection, and whether an application in routine diagnostic is reasonable.

NCT ID: NCT02051712 Recruiting - Clinical trials for Chronic Heart Failure

Cardiovascular Effects of Preferred Home-based Exercise Training in Systolic Heart Failure

HOMEX-HF-P
Start date: February 2014
Phase: Phase 3
Study type: Interventional

The aim of the study is I. To assess whether an individualized exercise training program is superior as compared to usual care with respect to exercise tolerance, II. to assess whether intervention tools that aim to increase exercise adherence are superior to an individualized exercise training alone with respect to exercise tolerance and long-term effects, and III. to identify biomarkers that that may be implemented into novel intervention tools aiming to increase exercise adherence in patients with chronic heart failure.

NCT ID: NCT02051621 Recruiting - Atrial Fibrillation Clinical Trials

Therapy of Atrial Flutter by Afib Ablation

TripleA
Start date: August 2010
Phase: N/A
Study type: Interventional

Ablation of the cavotricuspid isthmus (CTI) in the right atrium is currently the therapy of choice for the treatment of typical atrial flutter (3,4). It is a curative approach and has a high success rate (5). It has been recognized that patients with typical atrial flutter often complain of atrial fibrillation (1,2). Current clinical and experimental studies confirm the close relationship between atrial flutter (AFL) and atrial fibrillation (AF) and raise a question, if both arrhythmias are different forms of a common electrical phenomenon with atrial fibrillation being the underlying clinical problem (6).

NCT ID: NCT02045550 Recruiting - Clinical trials for Acute Wheezy Bronchitis

Tolerance and Effect of a Prophylactical Treatment With Ivy Leaves Dry Extract in Recurrent Wheezy Bronchitis

Start date: January 2014
Phase: Phase 2
Study type: Interventional

To evaluate the effect of a prophylactical therapy with a cough medicine containing ivy leaves dry extract on the frequency of recurrent wheezy bronchitis in toddlers, on the duration of the bronchitis episodes, on the severity and the additional drug demand. A prolonged asymptomatic episode between each wheezy bronchitis due to the therapy is assumed.

NCT ID: NCT02039479 Recruiting - Depression Clinical Trials

Randomized, Placebo-controlled Multicenter Trial of Lithium Plus Treatment as Usual (TAU) for Acute Suicidal Ideation and Behavior in Patients With Suicidal Major Depressive Episode

Start date: January 2014
Phase: N/A
Study type: Interventional

The primary hypothesis of this confirmatory study is that lithium therapy will acutely decrease suicidal ideation and/or suicidal behaviour in inpatients with a major depressive episode (MDE, unipolar and bipolar disorder according to DSM IV criteria). The specific aim is to test the hypothesis that lithium plus treatment as usual (TAU), compared to placebo plus TAU, results in a significantly greater decrease in suicidal ideation and/or behaviour over 5 weeks in inpatients with MDE.

NCT ID: NCT02034539 Recruiting - Quality of Life Clinical Trials

VADOplex Critical Limb Ischemia Study

Start date: October 2013
Phase: Phase 2/Phase 3
Study type: Interventional

In patients with critical limb ischemia (CLI) and foot ulcers wound healing is an important goal which can normally only be achieved after sufficient treatment of the underlying ischemia (revascularization either by an operation, e. g. bypass, or a catheter intervention). After successful revascularization everything should be done to improve wound healing because this regularly takes weeks up to several months. One possibility to speed up healing could be treatment with the VADOplex device which delivers an automatic intermittent painless compression of the sole of the foot thereby increasing perfusion of the leg. This system can be easily operated by patients themselves and at home. Our goal is to prove that the VADOPlex system accelerates healing up and improves quality of life.

NCT ID: NCT02033954 Recruiting - Bleeding Clinical Trials

Evaluation of Peripheral EOS for the Peripheral Embolization Treatment to Rapidly OccluDe Venous or Arterial BleEding

OCCLUDE-II
Start date: July 2014
Phase: N/A
Study type: Observational [Patient Registry]

To collect confirmatory data in support of the safety and performance of the ArtVentive Medical Group Endoluminal Occlusion System.

NCT ID: NCT02033811 Recruiting - Clinical trials for Mitral Regurgitation

MitraClip® Registry

Start date: January 2014
Phase:
Study type: Observational [Patient Registry]

Percutaneous mitral valve repair with the MitraClip® system has emerged as a therapeutic alternative to surgical valve repair (PMVR) in high risk patients. The aim of this registry is to collect prospectively and systematically clinical research data from patients undergoing PMVR with the MitraClip® system. This registry is an open-end observational study to assess the characteristics and outcomes patients with severe mitral regurgitation undergoing PMVR.

NCT ID: NCT02030327 Recruiting - Multiple Trauma Clinical Trials

Proteomics in Multiple Trauma to Identify Organ Failure

Start date: January 2014
Phase:
Study type: Observational

To analyse differences in protein expression in multiple trauma patients for identification of potential biomarkers to predict organ dysfunction.