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TEAS to Reduce Propofol Consumption During General Anesthesia

NCT02314650 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 162

Last updated 2022-11-14

No results posted yet for this study

Summary

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.

Conditions

  • Anesthesia

Interventions

OTHER

acupoint stimulation

stimulation was given at acupoints

OTHER

non-acupoint stimulation

stimulation was given at non-acupoints

OTHER

electrodes attached

electrode were attached to skin

Sponsors & Collaborators

  • Air Force Military Medical University, China

    lead OTHER

Principal Investigators

  • Zhihong LU, PhD · Air Force Military Medical University, China

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-08-25
Primary Completion
2017-12-28
Completion
2017-12-29

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02314650 on ClinicalTrials.gov