MedTrace Logo

Effects of Transcutaneous Acupoint Electrical Stimulation on Postoperative HRV and Hs-cTnT of Elderly With CHD

NCT03418194 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 137

Last updated 2019-05-13

No results posted yet for this study

Summary

The aim of this study was to observe the effect of transcutaneous acupoint electrical stimulation (TAES) on postoperative heart rate variability and high-sensitive cardiac troponin T of elderly patients with coronary heart disease.

Conditions

Interventions

PROCEDURE

transcutaneous acupoint electrical stimulation

Transcutaneous acupoint electrical stimulation(TAES) is a kind of noninvasive therapy similar to acupuncture and moxibustion. Its physiological effect is similar to that of electroacupuncture and hand acupuncture which is a Chinese traditonal therapy using acupuncture.

PROCEDURE

sham transcutaneous acupoint electrical stimulation

Sham transcutaneous acupoint electrical stimulation is the same procedure as transcutaneous acupoint electrical stimulation at points without electronic stimulation.

Sponsors & Collaborators

  • Hebei Medical University Third Hospital

    lead OTHER

Principal Investigators

  • Xiuli Wang, MD, PhD · Third Hospital of Hebei Medical Universit Department of Anesthesiology

  • Huizhou li, M.D · Third Hospital of Hebei Medical Universit Department of Anesthesiology

  • Chuan Wu, M.D · Third Hospital of Hebei Medical Universit Department of Anesthesiology

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2018-02-02
Primary Completion
2018-06-21
Completion
2018-06-30

Countries

  • China

Study Locations

More Related Trials

Entities

Diseases

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 NCT03418194 on ClinicalTrials.gov