Effects of taVNS Combined With Dexmedetomidine on POVN
The Effect of Dexmedetomidine Combined With Percutaneous Auricular Vagus Nerve Stimulation on Postoperative Nausea and Vomiting in Female Laparoscopic Patients: A Randomized Controlled Trial
- Postoperative Nausea and Vomiting
At a glance
- Phase
- Phase not stated
- Study type
- Interventional
- Sponsor
- Affiliated Hospital of Nantong University
- Enrolment target
- 176
- Started
- 7 December 2025
- Main results due
- 1 December 2026
- Study sites
- 1
- Registry updated
- 29 September 2026
Can you take part?
- Ages 18 years to 65 years.
- Women only.
- You need the condition being studied — healthy volunteers are not accepted.
These are the headline rules only. Every study has a longer list, and whether you are eligible is decided by the research team at the site — never by this page.
Read the full eligibility criteria
Inclusion Criteria: * Women aged 18 to 65; * Elective laparoscopic surgery under general anesthesia; * Classified as American Society of Anesthesiologists (ASA) physical status I to II; * 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 ASA anesthesia classification ≥ III; * Poorly controlled hypertension, atrioventricular block ≥ second degree, obesity (BMI \> 30 kg/m²); * Pregnant or breastfeeding; * Known allergy to drugs used in the study protocol, history of traumatic brain injury, history of gastrointestinal surgery; * Liver or kidney dysfunction (liver enzymes or creatinine ≥ 1.5 times the normal value), alcoholism or drug abuse, mental illness, use of antiemetics, opioids, psychoactive drugs, or corticosteroids within 24 hours before surgery; * Patients with implanted stimulators (such as pacemakers, implantable vagus nerve stimulators, deep brain stimulators, spinal cord stimulators, etc.), cochlear implants, or metal implants (except in dental cases); * Skin lesions or dermatological diseases at the site of electrical stimulation; * Preoperative heart rate \< 50 bpm or the presence of sinoatrial node disease or second-degree or higher atrioventricular block; * Patients unable to cooperate with assessments; * Patients participating in other clinical trials.
What this study is about
In the sponsor’s own words, from the registry.
To explore the effects and possible mechanisms of dexmedetomidine combined with taVNS on the incidence of postoperative nausea and vomiting in female patients undergoing laparoscopic surgery
Study sites(1)
Affiliated hospital of Nantong University
Nantong, Jiangsu, China
Recruiting
Showing 1 of 1 sites. 1 of the 1 site on this study is recruiting right now — a site can stop enrolling while the study as a whole is still open.
Source: ClinicalTrials.gov record NCT07271147. Trialion does not run this study, is not paid to refer anyone to it, and cannot enrol you. Eligibility is always decided by the research team at the site.
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