Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
50 participants
INTERVENTIONAL
2024-07-30
2025-05-07
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
DOUBLE
Study Groups
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transcutaneous electrical acupoint stimulation
Electrodes are placed at acupoints and connected to the stimulators. Electrical stimulation is given for 2 hours
transcutaneous electrical acupoint stimulation
Electrodes are placed at acupoints and connected to the stimulator. Electrical stimulation is given for 2 hours.
Control
Electrodes are placed at acupoints but no electrical stimulation is given
No interventions assigned to this group
Interventions
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transcutaneous electrical acupoint stimulation
Electrodes are placed at acupoints and connected to the stimulator. Electrical stimulation is given for 2 hours.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* History of severe respiratory, circulatory, digestive, blood, ear-nose-throat system diseases;
* A history of fever or respiratory infection within the last two weeks;
* Drinking alcohol or poor sleep within the last 24 hours
18 Years
50 Years
MALE
Yes
Sponsors
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Zhihong LU
OTHER
Responsible Party
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Zhihong LU
Associate professor
Locations
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Xijing Hospital
Xi'an, Shaanxi, China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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XJH-A-20240319
Identifier Type: -
Identifier Source: org_study_id
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