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Heart Failure clinical trials

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NCT ID: NCT03093012 Completed - Heart Failure Clinical Trials

Individual Blood Pressure Optimization Based on Cerebral Autoregulation After Implantation of Continuous-flow LVAD

NIRS
Start date: August 2015
Phase:
Study type: Observational

This study will collect retrospective and prospective clinical data regarding the Principal Investigator's patient population to allow for data analysis seeking basic trends and to prepare academic reports, including journal manuscripts and presentations for scientific organizations.

NCT ID: NCT03092284 Completed - Heart Failure Clinical Trials

Allogeneic Stem Cell Therapy in Heart Failure

CSCC_ASCII
Start date: September 2015
Phase: Phase 2
Study type: Interventional

The present aim is to perform at clinical double-blind placebo-controlled Cardiology Stem Cell Centre - Adipose Stem Cells (CSCC_ASC) study in heart failure patients to investigate the regenerative capacity of the CSCC_ASC treatment.

NCT ID: NCT03090724 Completed - Hypertension Clinical Trials

Pharmacokinetics of BIA 5-453 and Its Metabolites

Start date: June 13, 2008
Phase: Phase 1
Study type: Interventional

The purpose of this study was to assess the effects of age on the pharmacokinetic (PK) profile of BIA 5-453 and its metabolites.

NCT ID: NCT03090568 Completed - Hypertension Clinical Trials

Bioavailability Study of BIA 5-453

Start date: July 15, 2008
Phase: Phase 1
Study type: Interventional

The purpose of this study was to compare the bioavailability and tolerability of BIA 5-453 under fasted and fed conditions.

NCT ID: NCT03089281 Completed - Heart Failure Clinical Trials

Strategic Management to Optimize Response To Cardiac Resynchronization Therapy

SMART CRT
Start date: August 1, 2017
Phase: N/A
Study type: Interventional

The primary objective is to evaluate the benefit of the SmartDelayâ„¢ algorithm in patients with a prolonged RV-LV interval.

NCT ID: NCT03087773 Completed - Clinical trials for Acute Myocardial Infarction

Impact of EMpagliflozin on Cardiac Function and Biomarkers of Heart Failure in Patients With Acute MYocardial Infarction

EMMY
Start date: May 11, 2017
Phase: Phase 3
Study type: Interventional

This study is planned to investigate the impact of Empagliflozin on biomarkers of heart failure in patients with myocardial infarction with and without type 2 diabetes mellitus within 6 months after the event.

NCT ID: NCT03083301 Completed - Clinical trials for Cardiac Insufficiency

Cardiac Resynchronization Therapy: Relevance of the Surgical Approach in the Implantation of the Left Ventricular Probe

Start date: April 1, 2017
Phase:
Study type: Observational

Heart failure is very common and reaches more than 56 million people worldwide. 17 to 45 percent die in the first year of hospitalization. The most affected populations live in Western countries like Europe or the USA. It is defined by a set of signs and symptoms such as dyspnea, asthenia, edema or tachycardia but must be objectified, preferably by ultrasound. Its basic treatment is based on a lifestyle improvement and a reduction of the risk factors (hypertension, dyslipidemia, diabetes, ...), as well as an optimal medical treatment based on ACE inhibitors, B-blockers, ARA2 (Sartans), spironolactone or digoxin. When the optimal treatment is no longer working and that the cardiac desynchronization is demonstrated, be it atrio-ventricular, inter-ventricular or intra-ventricular, the patient can benefit from a three-probes cardiac resynchronization to resynchronize the two ventricles. The classic approach, performed by a cardiologist, is to perform an endovenous procedure in order to place the 3 probes under local anesthesia.The first one goes in the right atrium, the second one in the right ventricle and the third one goes in the left ventricle. It is the placement of this third one that often causes trouble. It is more difficult to place since it must pass through the coronary sinus, outside of the heart, unlike the first two probes that are placed endocavitary. When the practitioner fails to place the probe correctly or obtains inappropriate levels of detection, stimulation, or impedance thresholds, a cardiac surgeon must intervene and carry out a mini-thoracotomy. The CHU Brugmann Hospital is in favor of a mixed surgical approach. The probes are placed by a cardiac surgeon, who first starts by a endo-venous placement under local anesthesia. If that approach fails, the local anesthesia can be transformed into general anesthesia at the same operative time and a mini-thoracotomy is performed. The aim of this study is to evaluate the immediate impact of this surgical management within the CHU Brugmann hospital, in patients suffering from cardiac insufficiency despite proper medication.The hypothesis is that the mixed surgical approach improves the prognosis of cardiac resynchronization.

NCT ID: NCT03081052 Completed - Clinical trials for Heart Transplant Surgery

Inhaled Selective Pulmonary Vasodilators for Advanced Heart Failure Therapies and Lung Transplantation Outcomes

INSPIRE-FLO
Start date: May 4, 2017
Phase: Phase 4
Study type: Interventional

1. to conduct a clinical investigation to determine if inhaled epoprostenol (Veletri®, iEPO) and inhaled nitric oxide (iNO) will have similar impact on outcomes in adult patients undergoing durable LVAD placement, heart transplantation, or lung transplantation 2. to conduct a cost-capture analysis on the expense each drug incurs per patient.

NCT ID: NCT03079518 Completed - Iron Deficiency Clinical Trials

Intravenous Iron in paTients With Heart failURe and Reduced Ejection fracTion (HFREF) pLus Iron dEficiency

Iron Turtle
Start date: March 10, 2017
Phase: Phase 2
Study type: Interventional

Effects of ferric carboxymaltose single HD (1000 mg) infusion upon FGF23 in patients with isolated HFREF compared to patients with HFREF+CKD (all pts with iron deficiency). This study aims at identification of the optimal target population for a follow-up ("main") study.

NCT ID: NCT03077386 Completed - Hypertension Clinical Trials

Enhancing Community Health Through Patient Navigation, Advocacy and Social Support

ENCOMPASS
Start date: June 8, 2018
Phase: N/A
Study type: Interventional

Some patients who have multiple long-term health conditions have significant challenges accessing needed services despite available primary care and social services resources. Patient navigation programs may help those with complex health conditions improve their care and outcomes and if delivered by community health navigators (CHNs) who have close community ties, these programs have the potential to reduce barriers to care and increase access to coordinated, person-centred care. The ENCOMPASS program aims to improve the care and health outcomes for high-risk patients by linking patients with chronic disease with a CHN to help them navigate the health system, facilitate communication between patients and providers, improve patients' understanding of their conditions and treatment plans, and support patients in their self-management. In Canada, patient navigation programs have not been well studied or broadly implemented in patients with chronic disease, making a comprehensive evaluation of ENCOMPASS important. This program has great potential to improve care for patients with chronic diseases in primary care.