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Acupoint Stimulation Alleviates Postoperative Nausea and Vomiting

Effect of Transcutaneous Electrical Acupoint Stimulation on Postoperative Nausea and Vomiting After Liver Surgery

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05396716
Enrollment
158
Registered
2022-05-31
Start date
2022-05-30
Completion date
2023-05-30
Last updated
2022-05-31

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

Conditions

PONV

Keywords

transcutaneous electrical acupoint stimulation, liver surgery

Brief summary

Incidence of postoperative nausea and vomiting (PONV) could be high as 60% after liver surgery. Acupoint stimulation has been proved to decrease PONV. In this study, we will investigate the effect of transcutaneous electrical acupoint stimulation on incidence of PONV after liver surgery.

Interventions

DEVICEtranscutaneous electrical acupoint stimulation

Electrodes are placed at acupoints and connected to the stimulator. Electrical stimulation is given during surgery.

Sponsors

Zhihong LU
Lead SponsorOTHER

Study design

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

Masking description

The stimulator is put in an opaque box

Eligibility

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

Inclusion criteria

* age ≥18 years * scheduled for elective liver surgery under general anesthesia

Exclusion criteria

* body mass index less than 18 kg/m2 or higher than 30 kg/m2 * American Society of Anesthesiologists status higher than Ⅲ * patients with contraindication to transcutaneous electrical stimulation, including skin damage, infection or implantable electrical device * suspected or existed abuse of drug or alcohol * pregnant or breeding women * history of neurological or psychiatric disease

Design outcomes

Primary

MeasureTime frame
incidence of nausea and vomiting by 24 hours after surgeryfrom end of surgery to 24 hours after surgery, in a total of 24 hours

Secondary

MeasureTime frame
incidence of nausea and vomiting in PACU (post-anesthesia care unit)from end of surgery to discharge from PACU(post-anesthesia care unit), in an average of 30 minutes
score of nausea and vomiting by 24 hours after surgeryfrom end of surgery to 24 hours after surgery, in a total of 24 hours
score of nausea and vomiting by 48 hours after surgeryfrom end of surgery to 48 hours after surgery, in a total of 48 hours
score of nausea and vomiting in PACU(post-anesthesia care unit)from end of surgery to discharge from PACU, in an average of 30 minutes
incidence of nausea and vomiting by 48 hours after surgeryfrom end of surgery to 48 hours after surgery, in a total of 48 hours
Quality of recovery score at 48 hours after surgeryfrom end of surgery to 48 hours after surgery, in a total of 48 hours
postoperative in-hospital stayfrom end of surgery to discharge from hospital, in an average of 7 days
death by 6 months after surgeryfrom end of surgery to 6 months after surgery, in a total of 6 months
Quality of recovery score at 24 hours after surgeryfrom end of surgery to 24 hours after surgery, in a total of 24 hours

Contacts

Primary ContactZhihong Lu
deerlu23@163.com+8613891975018
Backup ContactShan He
1411950442@qq.com8684775343

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 21, 2026