Clinical Trials Directory

Trials / Unknown

UnknownNCT02597842

Transcutaneous Electrical Acupoint Stimulation(TEAS) for Postoperative Nausea and Vomiting in Laparoscopic Operation

Efficiency of Transcutaneous Electrical Acupoint Stimulation(TEAS) With Single Acupoint or Two Acupoints for Postoperative Nausea and Vomiting in Laparoscopic Operation: A Single Center, Randomized, Double-blinded, Controlled Clinical Trial

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
180 (estimated)
Sponsor
wangqiang · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This is a single center, randomized, double-blinded, controlled clinical trial.The purpose of this study is to compare the effect of TEAS pretreatment with single acupoint or two acupoints for postoperative nausea and vomiting in patients undergoing laparoscopic operation.

Detailed description

Patients were randomly assigned to four groups, receiving TEAS 30 minutes before induction.The stimulation was applied until the end of the operation. Postoperative nausea and vomiting was recorded 30 minute, 2 hour, 6 hour and 24 hour after the operation. The adverse events were recorded as well.

Conditions

Interventions

TypeNameDescription
DEVICETEAS (transcutaneous electrical acupoint stimulation)Electric stimulation was given through electrode attached to specific acupoints

Timeline

Start date
2015-12-01
Primary completion
2016-08-01
Completion
2016-10-01
First posted
2015-11-05
Last updated
2015-11-05

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02597842. Inclusion in this directory is not an endorsement.