Ear zaps may Kick-Start stomach after pancreatic surgery
NCT ID NCT06786923
First seen Jun 25, 2026 · Last updated Sep 02, 2026 · Updated 3 times
Summary
This study tested whether a device that gently stimulates the vagus nerve through the ear could reduce delayed stomach emptying after a major pancreatic surgery (pancreaticoduodenectomy). 84 patients were randomly assigned to receive the stimulation during surgery or not. The goal was to see if fewer patients would need a nasogastric tube or have trouble eating solid food a week after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- transcutaneous auricular vagus nerve stimulator (a device that stimulates the vagus nerve through the ear)
- What this could lead to
- If it works, this could offer a simple, non-drug way to help the stomach empty normally after pancreatic surgery, reducing hospital stays and discomfort.
- What could go wrong
- This is a small, single-center trial. The effect may be modest or not apply to all patients. The device may cause discomfort or fail to improve outcomes.
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
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84 people
The number who actually took part.
- Started
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Jan 2025
- Finished
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Oct 2025
- Lead sponsor
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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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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: * Age ≥18 years; * Diagnosed with pancreatic tumors or periampullary tumors by imaging or pathology and scheduled for pancreaticoduodenectomy; * No distant metastases and tumors are resectable; * Classified as American Society of Anesthesiologists (ASA) physical status I to III; * Capable of understanding the study procedures and various assessment scales and able to effectively communicate with the researchers; * Willing to participate in the study and provide written informed consent. Exclusion Criteria: * Patients with other malignant tumors; * Patients who have undergone chemotherapy or radiotherapy before surgery; * Patients with chronic organ dysfunction; * Patients with a history of gastrectomy or other gastric surgeries; * Patients diagnosed with chronic gastrointestinal inflammation, peptic ulcers, or a history of gastroparesis, pyloric, or other gastrointestinal obstructions; * Patients with a history of autonomic dysfunction (e.g., peripheral neuropathy, vagotomy, thyroid dysfunction, amyloidosis, asthma, heart failure, renal dysfunction, or alcoholism); * Patients with implanted stimulators (e.g., pacemakers, implanted vagus nerve stimulators, deep brain stimulators, spinal cord stimulators), cochlear implants, or metallic implants (excluding dental work); * Patients who recently used prokinetic agents, cholinergic or anticholinergic drugs, or hormones; * Patients who received vagus nerve stimulation or acupuncture within 1 month before the study; * Patients with skin damage or dermatological conditions at the stimulation site; * Patients with a preoperative heart rate below 60 beats per minute; * Patients unable to cooperate with assessments; * Patients participating in other clinical trials.
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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
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Affiliated hospital of Nantong University
Nantong, Jiangsu, 226001, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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