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Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 years
Awards & highlights
No Placebo-Only Group
Summary
This trial tests if using a portable lung ultrasound can help emergency medical personnel quickly and accurately diagnose heart failure in adults with severe shortness of breath.
Who is the study for?
This trial is for adults over 17 years old who are experiencing shortness of breath. It's not suitable for those with a high fever, pregnant women, patients with very low blood pressure, anyone showing certain heart attack signs on an EKG, or trauma patients.
What is being tested?
The study is testing if using lung ultrasound (LUS) in ambulances helps to diagnose acute heart failure better than the usual care without LUS. The goal is to see if this leads to quicker and more accurate treatment.
What are the potential side effects?
Since the intervention involves non-invasive lung ultrasound, there are minimal expected side effects compared to usual medical procedures; however, any discomfort or risks related to standard emergency care still apply.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 years
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Diagnostic accuracy of pre-hospital providers for identifying AHF versus not AHF
Secondary study objectives
Rate of initiation of AHF therapies in patients with AHF
Timing of AHF therapies in patients with AHF
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Group I: Usual CareExperimental Treatment1 Intervention
Group II: Lung UltrasoundExperimental Treatment1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Lung Ultrasound
2016
N/A
~1770
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Heart Failure (HF) include diuretics, which help reduce fluid overload and pulmonary congestion by promoting urine production; ACE inhibitors and angiotensin receptor blockers (ARBs), which lower blood pressure and decrease the heart's workload by inhibiting the renin-angiotensin-aldosterone system; beta-blockers, which slow the heart rate and reduce myocardial oxygen demand; and mineralocorticoid receptor antagonists, which further help in reducing fluid retention and preventing cardiac remodeling. These treatments are crucial for HF patients as they alleviate symptoms, improve quality of life, and reduce the risk of hospitalization and mortality.
The use of lung ultrasound (LUS) to detect B-lines can help in early identification of pulmonary congestion, allowing for timely and appropriate adjustments in HF management.
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Who is running the clinical trial?
Indiana UniversityLead Sponsor
1,035 Previous Clinical Trials
1,218,872 Total Patients Enrolled
18 Trials studying Heart Failure
3,756 Patients Enrolled for Heart Failure
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You have a fever higher than 100.4F.Adults over 17 years old who are experiencing shortness of breath as their main health concern.You have low blood pressure (SBP <90).You have a specific abnormality in your heart's electrical activity called ST-segment elevation on an EKG.People who have recently been injured are not eligible.
Research Study Groups:
This trial has the following groups:- Group 1: Usual Care
- Group 2: Lung Ultrasound
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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