Low Level Tragus Stimulation in Acute Decompensated Heart Failure (TREAT-HF)
Primary Purpose
Acute Decompensated Heart Failure
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Neuromodulation
Sponsored by
About this trial
This is an interventional treatment trial for Acute Decompensated Heart Failure
Eligibility Criteria
Inclusion Criteria:
Patients admitted with ADHF will undergo echocardiography which is considered standard of care. If estimated LVEF is 40% patients will be enrolled in the study.
Exclusion Criteria:
- Refusal to consent
- Complex congenital heart disease (Tetralogy of Fallot patients, single ventricle physiology)
- Recurrent vaso-vagal syncopal episodes
- Unilateral or bilateral vagotomy
- Sick sinus syndrome
- 2nd or 3rd degree AV block
- bifascicular block or prolonged 1st degree AV block (PR>300ms)
- Pregnant patients
- Prisoners
- Advanced renal dysfunction(defined as eGFR < 30, stage 4 or 5 chronic kidney disease)
- Hepatitis C or HIV
Sites / Locations
- OUHSCRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Tragus Stimulation
Control group
Arm Description
In this group patients will receive neuromodulation for 2 hours daily
Sham neuromodulation will be done
Outcomes
Primary Outcome Measures
Change in Interleukin (IL) levels
Interleukin level
Change in TNF-alpha levels
TNF level
Change in CRP levels
CRP level
Change in Pro BNP and renal function(creatinine) levels
Pro BNP level
Secondary Outcome Measures
Change in HRV
Heart rate variability measures such time and frequency domains
Full Information
NCT ID
NCT02898181
First Posted
September 1, 2016
Last Updated
August 24, 2023
Sponsor
University of Oklahoma
1. Study Identification
Unique Protocol Identification Number
NCT02898181
Brief Title
Low Level Tragus Stimulation in Acute Decompensated Heart Failure
Acronym
TREAT-HF
Official Title
Low Level Transcutaneous Tragus Stimulation to Reduce Inflammation, Dyspnea and Improve Heart Rate Variability in Acute Decompensated Heart Failure
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 2016 (undefined)
Primary Completion Date
September 2024 (Anticipated)
Study Completion Date
September 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Oklahoma
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Acute Decompensated Heart Failure (ADHF) is a major cause of morbidity and mortality. It is associated with increased systemic inflammation. Previous studies have demonstrated increased levels of cytokines such as C-reactive protein (CRP), interleukin-1 (IL-1), interleukin-6 (IL-6), interleukin-10 (IL-10) and Tumor Necrosis Factor alpha (TNFα) in patients with heart failure (HF). Increased activity of sympathetic nervous system in ADHF is linked to inflammation. Previous anti-inflammatory drug therapies in HF have demonstrated no significant impact on cardiovascular outcomes. Low-level vagus nerve stimulation (LLVNS) is a non-invasive way to modulate autonomic tone and thereby inflammation. Vagal nerve stimulation is thought to increase the parasympathetic activity and suppress the sympathetic activity. Clinical studies of vagal stimulation in chronic HF have been negative. Recent experimental and clinical data suggest that low level tragus nerve stimulation (LLTNS) may produce the same desired neuromodulator effect compared to LLVNS. It is however unknown if LLTNS in ADHF will directly lead to a reduction in the levels of pro-inflammatory cytokines (CRP, IL-1, IL-6 and TNF-α) and an increase in the level of anti-inflammatory marker IL-10. heart rate variability may also be abnormal in ADHF. The objective of this proposal is to determine the impact of LLTS on inflammatory cytokines, heart failure biomarkers(Pro BNP) and HRV in patients with ADHF.In addition we will study the impact on dyspnea resolution and change in renal function during hospitalization.
Patients will be randomized to either active or sham stimulation (2 hours daily). Serum collected will (post-admission and discharge day) will be used for cytokine measurement. We will also measure daily ECG to assess HRV and patient assessed dyspnea scale.This investigation will likely establish the first evidence of the effects of LLTS on the suppression of inflammation and improvement in dyspnea, natriuretic peptides, renal function and HRV in patients presenting with ADHF.
Detailed Description
Acute Decompensated Heart Failure (ADHF) is a major cause of morbidity and mortality. It is associated with increased systemic inflammation and poor outcomes.
Previous studies have demonstrated increased inflammation in patients with heart failure (HF). Increased activity of sympathetic nervous system in ADHF is linked to inflammation. Previous anti-inflammatory drug therapies in HF have demonstrated no significant impact on cardiovascular outcomes.
Low-level vagus nerve stimulation via stimulation of teh Tragus (LLTS) is a non-invasive way to modulate autonomic tone and thereby inflammation. Vagal nerve stimulation is thought to increase the parasympathetic activity and suppress the sympathetic activity. Recent experimental and clinical data suggest that low level tragus nerve stimulation (LLTS) may produce the same desired neuromodulator effect compared to LLVNS.
It is however unknown if LLTS in ADHF will directly lead to sympathetic tone reduction and increase in parasympathetic tone, or neuromodulation and lead to reduction in the levels of pro-inflammatory cytokines (CRP, IL-1, IL-6 and TNF-α) and an increase in the level of anti-inflammatory marker IL-10.
Autonomic tone could be assessed using heart rate variability. The objective of this proposal is to determine the impact of LLTS on inflammatory cytokines and HRV in patients with ADHF.
Patients will be randomized to either active or sham stimulation (2 hours daily).
Serum collected will (post admission and discharge day) will be used for cytokine and biomarker measurement. We will also measure 10-15 minute ECG to assess HRV. Dyspnea will be determined using patient assessment tool(visual analog scale).This investigation will likely establish the first evidence of effects of LLTS on suppression of inflammation and improvement in dyspnea scale, renal function and HRV in patients presenting with ADHF.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Decompensated Heart Failure
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Tragus Stimulation
Arm Type
Experimental
Arm Description
In this group patients will receive neuromodulation for 2 hours daily
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Sham neuromodulation will be done
Intervention Type
Device
Intervention Name(s)
Neuromodulation
Intervention Description
Active LLTS will be performed by use of a transcutaneous electrical nerve stimulation Parasym neuromodulation system with electrodes attached to the ear. Neuromodulation will be applied continuously for 2 hours daily.
Primary Outcome Measure Information:
Title
Change in Interleukin (IL) levels
Description
Interleukin level
Time Frame
From admission to discharge- over average 3-6 days
Title
Change in TNF-alpha levels
Description
TNF level
Time Frame
From admission to discharge- over average 3-6 days
Title
Change in CRP levels
Description
CRP level
Time Frame
From admission to discharge- over average 3-6 days
Title
Change in Pro BNP and renal function(creatinine) levels
Description
Pro BNP level
Time Frame
From admission to discharge- over average 3-6 days
Secondary Outcome Measure Information:
Title
Change in HRV
Description
Heart rate variability measures such time and frequency domains
Time Frame
From admission to discharge- over average 3-6 days
Other Pre-specified Outcome Measures:
Title
Change in level of dyspnea
Description
Dyspnea will be determined using simple tool called visual analog scale
Time Frame
From admission to discharge- over average 3-6 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients admitted with ADHF
Exclusion Criteria:
Refusal to consent
Complex congenital heart disease (Tetralogy of Fallot patients, single ventricle physiology)
Recurrent vaso-vagal syncopal episodes
Unilateral or bilateral vagotomy
Sick sinus syndrome
2nd or 3rd degree AV block
bifascicular block or prolonged 1st degree AV block (PR>300ms)
Pregnant patients
Prisoners
Advanced renal dysfunction(defined as eGFR < 30, stage 4 or 5 chronic kidney disease)
Hepatitis C or HIV
Acute Myocardial infarction
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tarun Dasari, MD,MPH
Phone
4052714742
Ext
44761
Email
tdasari@ouhsc.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tarun Dasari, MD,MPH
Organizational Affiliation
OUHSC
Official's Role
Principal Investigator
Facility Information:
Facility Name
OUHSC
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73104
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tarun Dasari
Phone
405-271-4742
Ext
44761
Email
tdasari@ouhsc.edu
First Name & Middle Initial & Last Name & Degree
Michael Stout
Phone
4052714742
Ext
44761
Email
michael-stout@ouhsc.edu
12. IPD Sharing Statement
Plan to Share IPD
No
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Low Level Tragus Stimulation in Acute Decompensated Heart Failure
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