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TEAS to Reduce Propofol Consumption During General Anesthesia (TOP)

A

Air Force Military Medical University of People's Liberation Army

Status

Completed

Conditions

Anesthesia

Treatments

Other: acupoint stimulation
Other: electrodes attached
Other: non-acupoint stimulation

Study type

Interventional

Funder types

Other

Identifiers

NCT02314650
XJH-A-2014-6-25-01

Details and patient eligibility

About

The study is aimed at whether transcutaneous electrical acupoint stimulation (TEAS) during general anesthesia could reduce the need for propofol in patients undergoing minor surgery.

Enrollment

162 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing minor surgeries including laparoscopic surgery and breast surgery under general anesthesia
  • Patients with written informed consent

Exclusion criteria

  • Patients with difficulty to communicate,including psychiatric disorder and Alzheimer's disease
  • Patients with drug abuse
  • Patients with disease of central nervous system
  • Patients with renal or hepatic dysfunction

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

162 participants in 3 patient groups, including a placebo group

Transcutaneous acupoint stimulation
Experimental group
Description:
Electrical stimulation was given through electrodes attached to skin at Ximen and Shenmen acupoint during anesthesia
Treatment:
Other: electrodes attached
Other: acupoint stimulation
Non-acupoint stimulation
Placebo Comparator group
Description:
Electrical stimulation was given through electrodes attached to skin at shoulder (non-acupoint) during anesthesia
Treatment:
Other: electrodes attached
Other: non-acupoint stimulation
Control
Sham Comparator group
Description:
patients were with electrodes attached but no stimulation was given
Treatment:
Other: electrodes attached

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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