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Electrical Acupoint Stimulation on Gastric Reflux During I-gel Ventilation

The Effect of Electrical Acupoint Stimulation on Gastric Reflux During Anesthesia With I-gel Ventilation

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07338448
Acronym
ASGARD-igel
Enrollment
116
Registered
2026-01-13
Start date
2026-01-12
Completion date
2026-07-31
Last updated
2026-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia

Keywords

acupoint stimulation, general anesthesia, gastric reflux, igel

Brief summary

This study will compare the effects of transcutaneous acupoint electrical stimulation versus no stimulation on intraoperative gastric reflux in patients undergoing general anesthesia with i-gel airway device ventilation.

Interventions

OTHERtranscutaneous electrical acupoint stimulation

electrical stimulation at 2Hz/10Hz is given from induction to end of surgery

Electrodes are pasted to the skin of Neiguan, Zusanli, Gongsun, Taichong acupoints

Sponsors

Air Force Military Medical University, China
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* age ≥18 years old * scheduled for surgery under general anesthesia with igel ventilation

Exclusion criteria

* American society of anesthesiologists status higher than grade 3 * history of gastrointestinal surgery * Currently taking acidic medications, or medications that affect gastric acid secretion or gastrointestinal motility * High risk of reflux or aspiration (e.g., symptomatic gastroesophageal reflux disease or hiatal hernia) * History of postoperative nausea and vomiting (PONV) * Intraoperative requirement of Trendelenburg position * Expected surgery duration exceeding 4 hours * Contraindications for acupoint electrical stimulation, such as patients with implanted electrophysiological devices, or skin infection/lesions at acupoint sites

Design outcomes

Primary

MeasureTime frame
pH value at middle-esophageal part at end of surgeryat end of surgery

Secondary

MeasureTime frame
number of gastric reflux episodesfrom intubation of igel to end of surgery, at an average of 2 hours
total duration of gastric reflux episodesfrom intubation of igel to end of surgery, at an average of 2 hours
longest duration of gastric reflux episodesfrom intubation of igel to end of surgery, at an average of 2 hours
pH value at glottis at the end of surgeryat end of surgery
percentage of patients suffering postoperative nausea and vomiting by 24 hours after surgeryfrom end of surgery to 24 hours after surgery

Contacts

Primary ContactZhihong Lu
deerlu23@163.com86-13891975018

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026