Research on E-Power Machine

E-Power Research

This E-Power clinical trial has been conducted by Convalescent Hospital of the Branch of Anhui Provincial Hospital in China for Insomnia and Arthrodynia requested by Anhui Provincial Medicine Supervision Bureau (File no.: 2004 Wan Yao Guan Xie No.03). Also another trial conducted by Affiliated Hospital to Bengbu School of Medicine, Anhui province for Rheumatoid Arthritis requested by the same bureau (File no.: 2004 Wan Yao Guan Xie No.05).

The age of the range for patients is from 18 to 65 combined with male and female. Here are how they conducted the trial and results:

By Convalescent Hospital of the Branch of Anhui Provincial Hospital in China

3Clinical Trial on Insomnia
30 people with Insomnia tried
All introduced to a 30 day trial with the administration of the E-Power twice a day according to the E-Power User's manual
Duration of each session varied from 30 minutes to 90 minutes
Intensity of stimulation varied according to person's tolerance level
2 days break were introduced after each 10 day cycle of assessment
Observations of symptom relief is based on 30 day period after the clinical trial completed

By Convalescent Hospital of the Branch of Anhui Provincial Hospital in China

Clinical Trial on Arthrodynia
- 30 people with Arthrodynia tried
All introduced to a 30 day trial with the administration of the E-Power twice a day according to the E-Power User's manual
Duration of each session varied from 30 minutes to 90 minutes
Intensity of stimulation varied according to person's tolerance level
2 days break were introduced after each 10 day cycle of assessment
Observations of symptom relief is based on 30 day period after the clinical trial completed

By Affiliated Hospital to Bengbu School of Medicine, Anhui, China

Clinical Trial on Rheumatoid Arthritis
30 people with Rheumatoid Arthritis tried
All introduced to a 30 day trial with the administration of the E-Power twice a day according to the E-Power User's manual
Duration of each session varied from 30 minutes to 90 minutes
Intensity of stimulation varied according to person's tolerance level
2 days break were introduced after each 10 day cycle of assessment
Observations of symptom relief is based on 30 day period after the clinical trial completed

Insomnia

	10th Day	20th Day	30th Day
Symptom Extinct	3.3%	20%	27%
Basically Extinct	13.3%	40%	43.3%
Symptom Improved	60%	23.3%	16.7%
No Result	23.3%	16.7%	13.3%

Arthrodynia

	10th Day	20th Day	30th Day
Symptom Extinct	3.3%	13.3%	20%
Basically Extinct	23.3%	36.7%	50%
Symptom Improved	53.3%	33.3%	20%
No Result	23.3%	16.7%	10%

Rheumatoid Arthritis - After 30 Day Treatment

Symptom Extinct	Basically Extince	Symptom Improved	No Result
16.7%	43.3%	33.3%	6.7%

Reference: HTE Newsletter Vol. 33 June 2011

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