A trial for improving effects of high-voltage electric potential on sleeplessness and low temperature

A trial for improving effects of high-voltage electric potential on sleeplessness and low temperature - A trial for improving effects of high-voltage electric potential on sleeplessness and low temperature

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000013166

Enrollment

Registered

2014-02-14

Start date

2013-03-26

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy adults

Interventions

Duration: 4 weeks Test product: SunMedion 30000MaxH, the generator of high-voltage electric potential Duration: 4 weeks no treatments

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: a) Males or postmenopausal women who are distressed by sleeplessness b) Persons who has chairs made of other than metal, or who can set the specific chairs which will be lent by provider of the test material

Exclusion criteria

Exclusion criteria: a) Persons who have previous medical history of heart failure or myocardial infarction b) Patients being treated for at least one of following diseases; atrial fibrillation, cardiac arrhythmia, hepatic disorder, renal disorder, cerebrovascular disorder, rheumatism, diabetes mellitus, dyslipidemia, hypertension, and other chronic disease c) Persons who take medicines, herbal medicines, or other therapeutic devices to treat severe pollinosis or by other reasons d) Persons who are applied medical electronic equipment (self-contained device such as pacemakers, life-supporting equipment such as cardiopulmonary bypass, wearable devices such as electrocardiograph) e) Persons who live with infants less than 1 years old f) Persons whose sleep period or sleeping habits are irregular due to night works or other reasons g) Persons who have been enrolled in the other clinical trials within last 3 months before the agreement for the participation to this trial h) Persons who are judged not suitable to participate in this trial by physician.

Design outcomes

Primary

Measure	Time frame
Sleep characteristics measured by SleepScan SL503 + Sleep Score + Ratio of deep sleep + Number of nocturnal awakening + Ratio of nocturnal awakening	—

Secondary

Measure	Time frame
Subjective symptoms + OSA sleep inventory MA version + Likert scales	—

Countries

Japan

Contacts

Public ContactNaoko SUZUKI

ORTHOMEDICO, Inc. R&D Department

nao@orthomedico.jp03-3818-0610

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026