ClinConnect ClinConnect Logo
Search / Trial NCT05230732

Neuromodulation of Inflammation and Endothelial Function

Launched by UNIVERSITY OF OKLAHOMA · Feb 4, 2022

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is looking at a new treatment method called low-level transcutaneous electrical stimulation (LLTS) of the vagus nerve to help patients with heart failure, specifically those with reduced heart function (known as heart failure with reduced ejection fraction, or HFrEF). The goal is to see if this treatment can improve symptoms, increase exercise ability, and enhance the quality of life for patients over a period of three months. By stimulating the vagus nerve, researchers hope to reduce inflammation and improve the function of blood vessels, which are often issues for people with heart failure.

To be eligible for this study, participants should be between the ages of 65 and 74 and have heart failure with a specific heart function measurement of 50% or less. However, individuals with certain conditions, such as recent severe heart problems, active cancer, or specific heart rhythm issues, cannot participate. Those who join the trial will receive LLTS for one hour a day over three months and will be monitored to see how this treatment affects their heart health and overall well-being. This research is important because it may lead to new, effective treatments for heart failure patients, especially as current options are sometimes limited.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Systolic heart failure with EF \< or equal to 50%.
  • Exclusion Criteria:
  • 1. patients in overt congestive heart failure / recent acute myocardial infarction (\< 4 weeks) or Unstable angina
  • 2. Active malignancy
  • 3. unilateral or bilateral vagotomy
  • 4. pregnant patients
  • 5. End stage liver disease
  • 6. history of recurrent vasovagal syncope, Sick sinus syndrome with no pacemaker, 2nd or 3rd degree AV block.
  • 7. Significant hypotension (Blood pressure \< 90 mm Hg) secondary to autonomic dysfunction

About University Of Oklahoma

The University of Oklahoma, a leading research institution, is dedicated to advancing healthcare through innovative clinical trials and research initiatives. With a robust network of interdisciplinary experts and state-of-the-art facilities, the university fosters an environment that promotes scientific discovery and the development of new treatments. Its commitment to patient-centered research ensures that clinical trials not only adhere to the highest ethical standards but also aim to address pressing health challenges. By collaborating with various stakeholders, including industry partners and healthcare providers, the University of Oklahoma seeks to translate research findings into tangible benefits for communities, ultimately enhancing the quality of care and improving health outcomes.

Locations

Oklahoma City, Oklahoma, United States

Oklahoma City, Oklahoma, United States

Patients applied

0 patients applied

Trial Officials

Tarun Dasari, MD, MPH

Principal Investigator

University of Oklahoma

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials