Clinical Trials Directory

Trials / Completed

CompletedNCT01930227

Transcutaneous Electrical Acupoint Stimulation(TEAS) for Hypotension After Spinal Anesthesia in Parturients

Effect of Transcutaneous Electrical Acupoint Stimulation(TEAS) on the Incidence of Hypotension After Spinal Anesthesia in Patients Undergoing Cesarean Section: a Prospective, Randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
150 (actual)
Sponsor
wangqiang · Academic / Other
Sex
Female
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the effect of TEAS on hypotension after spinal anesthesia in patients undergoing cesarean section

Detailed description

Patients were randomly assigned to 3 groups, receiving TEAS , non-acupoint stimulation or no-stimulation after spinal anesthesia respectively. 1.4 ml of bupivacaine mixed with 0.2ml of 50% glucose was given for spinal anesthesia under lateral position. Then the patient was switched to supine position and the OR table was tilted to the left for 15 degree. The sensory loss level was assessed. The blood pressure and heart rate every 2min were recorded for 30min after spinal anesthesia. The adverse events and use of ephedrine adverse events were recorded as well.

Conditions

Interventions

TypeNameDescription
OTHERTEASElectric stimulation was given through electrode attached to specific acupoints
OTHERNon-acupoint stimulationElectric stimulation was given through electrode attached to the shoulder

Timeline

Start date
2013-09-01
Primary completion
2014-08-01
Completion
2014-08-01
First posted
2013-08-28
Last updated
2014-12-09

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT01930227. Inclusion in this directory is not an endorsement.