Condition
Congestive Heart Failure (CHF)
ClinicalTrials.gov condition label
Clinical trials
16 shownThe FILTRATE Trial: High-Rate Ultrafiltration for Intravascular CongestionNCT07705269 · 2026-06-04
RECRUITINGPalliative Care for People With HFNCT07356843 · 2025-10-29
RECRUITINGEvaluation of the Use of Empagliflozin in Patients with HF with PEF in a Cardiology Outpatient DepartmentNCT06683053 · 2023-03-17
ACTIVE_NOT_RECRUITINGDeveloping Enhanced Prediction ModelsNCT02983812 · 2017-01-23
COMPLETEDClinical Trials for Elderly Patients With Multiple DiseaseNCT01960907 · 2013-10-01
COMPLETEDExpanding Paramedicine in the CommunityNCT02034045 · 2013-06-01
COMPLETEDPulmonary Blood Flow Measurements in CHF PatientsNCT01831713 · 2012-09-01
TERMINATEDEvaluation of Blood Flow Patterns in Lung Blood Vessels Using Ultrasound Technique in Patients With Congestive Heart FailureNCT01744210 · 2012-09-01
WITHDRAWNGroup Psychotherapy Among Congestive Heart Failure PatientsNCT01414439 · 2011-08-01
UNKNOWNOutlook Quality of Life Intervention StudyNCT01044290 · 2011-01-01
COMPLETEDA Trial to Reduce Readmissions Using Motivational Interviewing and Interactive Voice ResponseNCT01855022 · 2010-06-01
COMPLETEDProspective Evaluation of the StatusFirst™ CHF NT-proBNP Device in Human Whole Blood and Plasma SamplesNCT00734045 · 2008-02-01
COMPLETEDRecombinant Human Relaxin for the Treatment of Decompensated CHFNCT00406575 · 2006-11-01
TERMINATEDCHF Management Using TelemedicineNCT00309764 · 2001-11-01
COMPLETEDImproving Heart Failure Care in Minority CommunitiesNCT00211874 · 2000-09-01
COMPLETEDClinical Evaluation of Cardiac Resynchronization Therapy (CRT) Using the Ovatio CRT Implantable Cardioverter-defibrillator (ICD) SystemNCT00528320
APPROVED_FOR_MARKETINGCommon interventions
ADAPTOTHER1Attention ControlOTHER1CHROMED monitoring systemDEVICE1Community ParamedicineOTHER1empagliflozinDRUG1Existential Group TherapyBEHAVIORAL1High-rate ultrafiltrationPROCEDURE1Life CompletionOTHER1MI + IVRBEHAVIORAL1Nurse-managementBEHAVIORAL1Ovatio CRTDEVICE1PlaceboDRUG1Recombinant human relaxin (rhRlx)DRUG1Standard fluid removalPROCEDURE1TelemedicineBEHAVIORAL1Usual CareOTHER1
Leading sponsors
Echosense Ltd.2Asante Health System1Conrado Roberto Hoffmann Filho1Corthera, Inc.(formerly BAS Medical, Inc.), a member of the Novartis group of companies1ELA Medical, Inc.1Icahn School of Medicine at Mount Sinai1Indiana University1Kaiser Permanente1Meir Medical Center1Nanogen, Inc.1Restech Srl1Unity Health Toronto1Universidad Autonoma de Nuevo Leon1University of Pennsylvania1VA Office of Research and Development1
Trial status mix
COMPLETED8
RECRUITING2
TERMINATED2
ACTIVE_NOT_RECRUITING1
APPROVED_FOR_MARKETING1
UNKNOWN1
WITHDRAWN1
Phase mix
NA7
PHASE21
PHASE31
Registry-derived research relationships: ClinicalTrials.gov. Raw condition and intervention labels remain distinct from canonical MONDO/RxNorm entities unless separately normalized.