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NCT04621578

Transcutaneous Electrical Acupoint Stimulation on Postoperative Dizziness in Hemifacial Spasm Patients

Completed NA Last updated 1 June 2022
What this trial tests

NA trial testing HANS 100B stimulator (4 conductors, 8 electrodes; Jisheng Co., Nanjing, China) in Transcutaneous Electrical Acupoint Stimulation in 86 participants. Completed in 30 July 2021.

Timeline
6 December 2020
Primary endpoint
25 June 2021
30 July 2021

Quick facts

Lead sponsorPeking University People's Hospital
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment86
Start date6 December 2020
Primary completion25 June 2021
Estimated completion30 July 2021
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Peking University People's Hospital

Who can join

Adults 18 to 70, any sex, with Transcutaneous Electrical Acupoint Stimulation or Hemifacial Spasm. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To observe the prevention and treatment effect of transcutaneous electrical acupoint stimulation (TEAS) on postoperative dizziness in patients with hemifacial spasm undergoing microvascular decompression surgery, and its possible mechanisms.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Peking University People's Hospital trials

Trials by the same sponsor.

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Data sources for this page

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