What this study is
Sepsis is life-threatening organ dysfunction caused by a dysregulated host response to infection. It is the most expensive healthcare condition to treat in United States and has a mortality rate of nearly 30%. It is widely known that exaggerated inflammation and imbalance between sympathetic and parasympathetic arms of the autonomic nervous system (ANS) contribute to progression and adverse outcomes in sepsis. The role of unchecked inflammation and unregulated ANS as a potential treatment target is an important gap in our knowledge that should be explored.
Cholinergic anti-inflammatory pathway (CAP) is an intricate network where the ANS senses inflammation by vagus nerve afferents and tries to regulate it by vagus nerve efferents to the reticuloendothelial system. The central hypothesis of this pilot clinical trial is that transcutaneous vagus nerve stimulation (TVNS) at tragus of the external ear can activate the CAP to suppress inflammation and improve autonomic imbalance as measured by inflammatory cytokine levels and heart rate variability (HRV) analysis. The investigators plan to randomize patients with septic shock into active and sham stimulation groups and study the effects of vagal stimulation on inflammatory cytokines, HRV and a clinical severity score of sepsis. Both groups will continue to receive the standard of care treatment for sepsis irrespective of group assignments. The investigators hypothesize that 4 hours of TVNS will suppress inflammatory markers and improve the balance between sympathetic and parasympathetic arms of ANS as measured by HRV, resulting in improved Sequential Organ Failure Assessment Score (SOFA). The preliminary data generated from this pilot study will lay the foundation for a larger clinical trial.
What's being tested
- Low Level Transcutaneous Vagus Nerve Stimulation
Intervention · DEVICE
Stimulation of the auricular branch of the vagus nerve at tragus of the external ear delivered by Parasym device.
- Low Level Transcutaneous Vagus Nerve Stimulation
Intervention · DEVICE
Stimulation of the ear lobe delivered by Parasym device.
Study details
- Sponsor
- University of Oklahoma
- Conditions
- Septic Shock
- Enrolling
- 34 people
- Starts
- 2019-10-10
- Est. completion
- 2027-12
- Design
- Double-blind, randomized, parallel groups
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years and overSex ALLHealthy volunteers Not acceptedYou may qualify if
- Septic shock (meeting severe sepsis and having persistent systolic blood pressure <90mmHg despite adequate fluid resuscitation).
You can't join if
- Unilateral or bilateral vagotomy
- History of myocardial infarction or stroke in the last 1 year
- Recurrent vasovagal syncope
- Sick sinus syndrome without pacemaker
- Bifascicular heart block
- 2nd or 3rd-degree heart block
- Hypotension due to autonomic dysfunction
- Pregnant women
- Prisoners and patients with suicidal ideation
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openUniversity of Oklahoma Health Sciences Center
Oklahoma City, Oklahoma, United States
- Houssein Youness, MD · Contact405-271-6173Houssein-Youness@ouhsc.edu
Recruiting
Study team
Sponsor
University of Oklahoma
Study ID 9227
Principal investigator
Houssein Youness, MD
University of Oklahoma
Principal investigator
Zain Ul Abideen Asad, MD
University of Oklahoma
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.