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
| Type | Name | Description |
|---|---|---|
| OTHER | TEAS | Electric stimulation was given through electrode attached to specific acupoints |
| OTHER | Non-acupoint stimulation | Electric 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.