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Chronic Heart Failure clinical trials

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NCT ID: NCT03615157 Recruiting - Clinical trials for Chronic Heart Failure

Effects of a Home-based Exercise Program on Functional Capacity and Quality of Life in Heart Failure Patients

Start date: January 15, 2018
Phase: N/A
Study type: Interventional

Heart failure (HF) is a multisystemic disease leading to exercise intolerance and fatigue. Supervised physical training improves functional capacity, quality of life and reduces hospital admissions in HF patients. In this way, home physical training may be a good alternative to patients who, for any reason, cannot perform supervised training. Objective: To asses the effects of a home-based training program on functional capacity, sedentary lifestyle and quality of life of patients with chronic HF compared to supervised training.

NCT ID: NCT03388593 Recruiting - Clinical trials for Chronic Heart Failure

Survival Study of the Recombinant Human Neuregulin-1β in Subjects With Chronic Heart Failure.

Start date: July 23, 2018
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate efficacy of rhNRG-1 in reducing the death rate of heart failure subjects with baseline NT-proBNP level between 600 pg/ml and 1700 pg/mL and NYHA class II to III.

NCT ID: NCT03333499 Recruiting - Clinical trials for Chronic Heart Failure

the Effects of YangXinShi (YXS) on the Quality of Life and Exercise Tolerance in Patients With Chronic Heart Failure

Start date: November 1, 2017
Phase: Phase 1
Study type: Interventional

The investigators set out to evaluate the effects of the traditional Chinese medicinal mixture under the brand name YangXinShi (YXS) on the prognosis in patients with chronic heart failure when it is combined with the optimal combination drug treatment of heart failure.

NCT ID: NCT03286127 Recruiting - Cancer Clinical Trials

Palliative Outcome Evaluation Muenster I

POEM I
Start date: September 11, 2017
Phase:
Study type: Observational

For patients with an advanced disease and their families an excellent and compassionate care is essential. However, in hospitals optimal end-of-life care is not yet fully realized and patient's needs are often not met. Palliative care is able to increase patients' quality of life and to carefully meet their and their families' needs. To improve the awareness of unmet needs patient-reported outcome measurement has been the pivot of latest palliative care research. Besides the improvement of care outcome measurement allows the evaluation of the quality of palliative care and comparisons on a national and international level. The aim of the present study is to evaluate the quality of palliative care in different settings (palliative care unit, inpatient and outpatient consultation teams) using the Integrated Palliative Care Outcome Scale (IPOS). The IPOS has been lately developed as improved follow-up version of the Palliative Care Outcome Scale (POS) integrating most important questions and simultaneously being brief and comprehensive. The study is planned as a multi-centric observational study. Primary endpoint is the reduction of symptom burden of patients. The clinical study hypothesis bases on the assumption that palliative care can change the symptom burden, measured by a change in the IPOS overall profile score, and that there might be a difference in the size of the effect depending on the caring setting.

NCT ID: NCT03254212 Recruiting - Clinical trials for Chronic Heart Failure

Nocturnal Oxygen Needs and Central Sleep Apnea in Patients With Chronic Heart Failure.

HO2F
Start date: April 15, 2018
Phase: Phase 4
Study type: Interventional

The aims of this study are to 1) determine the optimal levels of O2 flow which prevent nocturnal O2 desaturation while minimizing periods of hyperoxia during the course of nocturnal oxygen therapy (NOXT) in heart failure patients with reduced ejection fraction (HFrEF) patients with CSA/CSR; 2) document whether within-patient EO2F values change over time during NOXT, and identify factors which predict changes in EO2F; and 3) examine how well a conventional stepwise titration procedure compares to a breath by breath titration using an automated O2 titration system in terms of targeted flow rate and night time oxygenation (oxygen desaturation index, time spent at specific SpO2 targets).

NCT ID: NCT03153774 Recruiting - Sarcopenia Clinical Trials

Assessments of Sarcopenia Prevalence in Chronic Heart Failure Patients and in Subjects Before TAVI

PRESAR-HF
Start date: November 3, 2014
Phase: N/A
Study type: Interventional

The main objective was to assess the prevalence of sarcopenia in chronic heart failure patients and in patients before the trans aortic valvular implantation. The loss of muscle mass in chronic heart failure patients is a prognostic factor for sarcopenia. The purpose was to identify in these patients signs of sarcopenia for a better management.

NCT ID: NCT03125720 Recruiting - Clinical trials for Chronic Heart Failure

Image Fusion of SPECT MPI and Fluoroscopy Venography to Guide LV Lead Placement for Improved CRT Response (GUIDE-CRT II)

GUIDE-CRT
Start date: April 14, 2017
Phase: N/A
Study type: Interventional

CRT response will be significantly better using image fusion of SPECT MPI and fluoroscopy venogram to guide LV lead placement at the latest activation segment without scar than standard-of-care implantation.

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.

NCT ID: NCT02970214 Recruiting - Metabolic Syndrome Clinical Trials

Follow-up of GANI_MED Cardio Cohorts

GANIFU-Card
Start date: November 2016
Phase:
Study type: Observational [Patient Registry]

Follow-up of two hospital-based patient cohorts (heart failure, metabolic comorbidities in CVD), recruited at baseline by the GANI_MED-project (Greifswald Approach to Individualized Medicine). Standardized protocols will be used for the assessment of medical history, laboratory biomarkers, and the collection of various biosamples for bio-banking purposes. Comparisons with the general background population will be performed.

NCT ID: NCT02794935 Recruiting - Clinical trials for Chronic Heart Failure

The Effects of Inspiratory Muscle Training in Patients With Heart Failure and Obstructive Sleep Apnea Syndrome

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

This research aims to evaluate the effects of inspiratory muscle training (IMT) on apnea hypopnea index, sleepiness, sleep quality, cognitive function, motor task, executive function, quality of life, chemoreflex sensitivity and vagal modulation of heart rate in patients with heart failure and obstructive sleep apnea syndrome.