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Impact of Clinical Ultrasound in Patients With Heart Failure Treated in Home Hospitalization (AHF-CU)

Primary Purpose

Acute Heart Failure (AHF)

Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
CLINICAL ULTRASOUND
Sponsored by
Lara Palacios
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Heart Failure (AHF) focused on measuring Acute heart failure, Ultrasound, Hospital at home, Readmision

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • AHA documented
  • HAH admission
  • Informed consent
  • 2 or more CU on the intervention group being one the day of admission

Exclusion Criteria:

  • Life expectancy below 6 months
  • Active tumors
  • Interstitial lung disease
  • Respiratory distress
  • Pulmonary concussion
  • Inotropic drugs on admission
  • Patients coming from intensive care unit
  • Intolerance or allergy to diuretic treatment

Sites / Locations

  • Hospital Reina SofiaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

No intervention arm

Experimental arm

Arm Description

Standard care of AHF on a patient admitted on a HAH unit consists in physical examination and basic complementary tests

Clinical ultrasound on HAH admitted patient. Clinical handheld Ultrasound consists of inferior vena cava diameter measurement and lung ultrasound protocol in order to guided Diuretic Therapy

Outcomes

Primary Outcome Measures

Readmission due to AHF
Admission on the internal medicine ward for more than 24 hours due to AHF after being discharge from the AHA unit. We do not consider admission in the emergency room due to AHF after being discharge from the AHA unit.
Mortality due to AHF
Death related to an AHF episode after being discharge from the AHA unit.

Secondary Outcome Measures

Readmission due to a cause different to AHF.
Admission on the internal medicine ward for more than 24 hours after being discharge from the AHA unit due to a cause different to AHF. We do not consider admission in the emergency room after being discharge from the AHA unit due to a cause different to AHF
Mortality due to a cause different to AHF
Any death related to a cause different to AHF after being discharge from the AHA unit.

Full Information

First Posted
September 3, 2021
Last Updated
September 23, 2021
Sponsor
Lara Palacios
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1. Study Identification

Unique Protocol Identification Number
NCT05042752
Brief Title
Impact of Clinical Ultrasound in Patients With Heart Failure Treated in Home Hospitalization
Acronym
AHF-CU
Official Title
Impact of Clinical Ultrasound in Patients With Heart Failure Treated in Home Hospitalization (AHF-CU)
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2021 (Actual)
Primary Completion Date
January 1, 2022 (Anticipated)
Study Completion Date
March 1, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Lara Palacios

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to assess whether clinical ultrasound (CU)-guided treatment in acute heart failure (AHF) is superior to the standard care (SC)-guided treatment. We would like to see if using a portable ultrasound to guide diuretic therapy for AHF patients will prevent hospital readmissions in the setting of hospitalization at home (HAH). This study will use a handheld ultrasound called IVIZ-Sonosite and aims to see whether changing diuretic therapy based on the performance of the ultrasound will result in the less hospitalizations for heart failure as compared to performing just SC-guided therapy.
Detailed Description
AHF remains a leading cause of death in industrialized countries. Despite advances in medical treatment, an estimated 250,000-300,000 AHF patients are hospitalized in the United States each year for symptoms caused by low cardiac output. Although the events that cause acute decompensation are multifactorial, the common pathway associated with decreased ventricular function are autonomic dysfunction and fluid retention. It has been previously suggested that an estimated 50%-66% of CHF hospitalizations may be preventable with improved monitoring of fluid volume status. In Spain, more than 10% of discharged patients are readmitted within 30 days. AHF is one of the most frequent reasons for readmission, mainly because of congestion-related symptoms. The size and shape of the inferior vena cava and the presence of B lines have proven to be effective to estimate volume overload and to guide diuretic treatment in AHF on a hospital setting. At the same time, technology is quickly evolving and new approaches for clinical care are arising. The aim of this study is two compare SC-guided therapy vs CU-guided therapy in AHF patients admitted on a HAH. We designed an open label clinical trial, in which patients are randomized into two groups: "ultrasound group" who undergoes CU together with SC and "control group" who undergoes SC only. Diuretic treatment will be tailored according to the findings of the SC together with the CU or according to the findings of the SC respectively. A total of 140 patients will be recruited, 70 patients on each arm. The outcome variables are readmission for AHF and other causes, mortality for AHF and other causes, and the combined event of readmission for AHF and mortality for AHF at one month and two months. The CU protocol will include both lung ultrasound and inferior vena cava measurement and will be performed with an ultraportable device (IVIZ-Sonosite). Standard care will involve physical examination and basic complementary tests. The way patients end up admitted to HAH are transferences from the emergency room, from the internal medicine ward, from the clinics and from primary care. During admission, daily visits are carried out by the nursing staff (except when clinical stability and no need to intravenous treatment infusions) and every two days by the medical team. Admission in the HAH is always voluntary and patients can decide to return to hospital during HAH stay. In the HAH unit, there is a 24-hour telephone service coordinated by a specialized nurse on call.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Heart Failure (AHF)
Keywords
Acute heart failure, Ultrasound, Hospital at home, Readmision

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
140 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
No intervention arm
Arm Type
No Intervention
Arm Description
Standard care of AHF on a patient admitted on a HAH unit consists in physical examination and basic complementary tests
Arm Title
Experimental arm
Arm Type
Experimental
Arm Description
Clinical ultrasound on HAH admitted patient. Clinical handheld Ultrasound consists of inferior vena cava diameter measurement and lung ultrasound protocol in order to guided Diuretic Therapy
Intervention Type
Procedure
Intervention Name(s)
CLINICAL ULTRASOUND
Intervention Description
The intervention group will receive the standard care of treatment in AHF and the performance of CU.
Primary Outcome Measure Information:
Title
Readmission due to AHF
Description
Admission on the internal medicine ward for more than 24 hours due to AHF after being discharge from the AHA unit. We do not consider admission in the emergency room due to AHF after being discharge from the AHA unit.
Time Frame
At 30 days and 60 days
Title
Mortality due to AHF
Description
Death related to an AHF episode after being discharge from the AHA unit.
Time Frame
At 30 days and 60 days
Secondary Outcome Measure Information:
Title
Readmission due to a cause different to AHF.
Description
Admission on the internal medicine ward for more than 24 hours after being discharge from the AHA unit due to a cause different to AHF. We do not consider admission in the emergency room after being discharge from the AHA unit due to a cause different to AHF
Time Frame
At 30 days and 60 days
Title
Mortality due to a cause different to AHF
Description
Any death related to a cause different to AHF after being discharge from the AHA unit.
Time Frame
At 30 days and 60 days.
Other Pre-specified Outcome Measures:
Title
Cumulative event
Description
At least one AHA readmission or mortality due to AHA
Time Frame
At one or two months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: AHA documented HAH admission Informed consent 2 or more CU on the intervention group being one the day of admission Exclusion Criteria: Life expectancy below 6 months Active tumors Interstitial lung disease Respiratory distress Pulmonary concussion Inotropic drugs on admission Patients coming from intensive care unit Intolerance or allergy to diuretic treatment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
LARA PALACIOS GARCIA, MD
Phone
+(34) 8484434000
Ext
51067
Email
lara.palacios.garcia@navarra.es
First Name & Middle Initial & Last Name or Official Title & Degree
RUTH GARCIA REY
Phone
+(34) 848422163
Email
ruth.garcia.rey@navarra.es
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
LARA PALACIOS GARCIA, MD
Organizational Affiliation
Hospital Reina Sofia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Reina Sofia
City
Tudela
State/Province
Navarra
ZIP/Postal Code
31500
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
LARA PALACIOS GARCIA, MD
Phone
+(34) 8484434000
Ext
51067
Email
lara.palacios.garcia@navarra.es
First Name & Middle Initial & Last Name & Degree
RUTH GARCIA REY
Phone
+(34) 848422163
Email
ruth.garcia.rey@navarra.es
First Name & Middle Initial & Last Name & Degree
LARA PALACIOS GARCIA, MD
First Name & Middle Initial & Last Name & Degree
PABLO RUIZ SADA, MD

12. IPD Sharing Statement

Plan to Share IPD
No

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Impact of Clinical Ultrasound in Patients With Heart Failure Treated in Home Hospitalization

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