Scientists map vagus nerve stimulation to reduce side effects in epilepsy
NCT ID NCT05395026
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This study tested different settings of vagus nerve stimulation (VNS) in 16 adults with epilepsy who were already scheduled for VNS device surgery. Researchers measured how stimulation affected heart rate and throat muscle contractions to find ways to reduce side effects. The goal is to improve future VNS programming for better epilepsy control with fewer discomforts.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- electrical stimulation of the vagus nerve
- What this could lead to
- If successful, this could help doctors fine-tune VNS devices to reduce side effects like throat muscle contractions and heart rate changes.
- What could go wrong
- This is a small, early-stage study with only 16 participants, focused on measuring effects rather than testing a new treatment. Results may not apply to all epilepsy patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
16 people
The number who actually took part.
- Started
-
Nov 2022
- Finished
-
Jul 2024
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 65 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * adult epilepsy patients undergoing VNS electrode implantation or implanted pulse generator (IPG) replacement surgery * in good health * neurologically stable aside from epilepsy * able to provide informed consent Exclusion Criteria: * patients with another implanted electrical device (besides VNS) * a history of heart conditions that the surgeon considers a contraindication to study participation
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Epilepsy are added.
By submitting, you agree to our Terms of use
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Duke University Medical Center
Durham, North Carolina, 27710, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Brain regions and functional neuronal network characteristics of dexmedetomidine analgesia under intraoperative fMRI
- Can stem cells boost brain surgery for epilepsy?
- Can brain stimulation unlock the secret to erasing fear?
- Can brain electrodes reveal the signatures of thought?
- Mozart's sonata may tame seizures in children
- Can a scalp device quiet deep brain circuits? a new study investigates