A Single Center Pilot Study on the Use of a Transcutaneous Auricular Vagus Nerve Stimulation Device in CKD Population

Brief description of study

This study aims to gather initial data on the potential effectiveness of a transcutaneous auricular vagal nerve stimulation device in patients diagnosed with chronic kidney disease. The study participants will receive a 15-minute session of transcutaneous auricular vagal nerve stimulation at one of two specified doses, assigned alternatively. Prior to and after the stimulation, vital signs, heart rate variability, and autonomic function will be monitored. Our primary aims are to investigate the feasibility of the protocol and generate preliminary signals of efficacy and tolerability for two different doses of vagal nerve stimulation. The pilot estimates will be used to design a larger scale study that may lead to potentially targeted interventions to reduce CV mortality in the CKD population.


Clinical Study Identifier: s23-00778
ClinicalTrials.gov Identifier: NCT05981183
Principal Investigator: David Michael Charytan.
Other Investigator: Qandeel Haq Soomro.


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