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Portable Ultrasound to Predict Heart Failure Readmission Risk

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The Guthrie Clinic

Status

Withdrawn

Conditions

Patient Readmission
Heart Failure

Treatments

Diagnostic Test: Ultrasound

Study type

Interventional

Funder types

Other

Identifiers

NCT05980533
2307-41

Details and patient eligibility

About

The purpose of this research is to use a handheld ultrasound to assess patients with congestive heart failure (CHF) to see if the ultrasound can help predict readmission to the hospital. The study will include patients who are admitted to the hospital for CHF. Participants will have two ultrasounds at hospital discharge and at a follow up visit.

Full description

The purpose of this research is to see if a portable ultrasound can help predict readmission to the hospital for patients who are admitted to the hospital for CHF. The study will enroll patients who take part in Mobile Integrated Healthcare as part of their routine care. Participants will have two ultrasounds. The first ultrasound will be at hospital discharge.

Between seven to ten days after hospital discharge participants will be visited at their home in follow-up as the usual standard of care for Mobile Integrated Healthcare. At this visit participants will have a second ultrasound. Participants will be followed for one year for hospital readmission.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Primary admission diagnosis is listed as congestive heart failure, with an acute component of decompensation.
  • Age greater than 18 years.
  • Principal residence within the geographic reach of our MIH program.

Exclusion criteria

  • pregnant women

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

0 participants in 1 patient group

Ultrasound
Experimental group
Description:
Ultrasound at hospital discharge and at follow up in 7-10 days
Treatment:
Diagnostic Test: Ultrasound

Trial contacts and locations

0

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Central trial contact

Zachary Dewar, MD

Data sourced from clinicaltrials.gov

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