EFFECTS OF RejuvaMatrix ™ ON TELOMERES

NCT ID: NCT04048044

Last Updated: 2019-08-07

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-01-31

Study Completion Date

2014-12-31

Brief Summary

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Lying for 30 to 60 minutes daily in a field of 75 decibels of electromagnetic energy at 54 to 78 GHz will allow telomeres of white blood cells to regenerate

Detailed Description

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Individuals who are post menopausal and who do not have an implanted electronic device, such as a pacemaker will have base line white blood cell telomeeres measured at Repeat Diagnostics in Vancouver. They will be supplied with a two inch foam mat in the center of which is copper screen with one pound of crushed sapphire. The mat looks like a mattreess and is placed on top of the regular mattress. Participants are provided with a Tesla coil to be attached to a copper wire coming from the copper screen. They will also be provided with a timer so that they can set the Tesla coil to be activated for a maximum of 60 minutes while they sleep.

Telomeres will be measured at the end of each year for 5 years.

Conditions

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Telomeres

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Telomere length, GigaHz exposure

Measurement of white blood cell telomeres before and yearly for 5 years

Group Type ACTIVE_COMPARATOR

Exposure to GHz electromagnetic energy (RejuvaMatrix)

Intervention Type DEVICE

75 decibels of 54 to 78 GHz daily for 60 minutes

Interventions

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Exposure to GHz electromagnetic energy (RejuvaMatrix)

75 decibels of 54 to 78 GHz daily for 60 minutes

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

\-

Exclusion Criteria

* Implanted electronic device
* Major, debilitating disease
* Person living with an individual who has an implanted device
* Person who is or could become pregnant
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Holos Institutes of Health, Inc

OTHER

Sponsor Role lead

Responsible Party

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C. Norman Shealy

M.D., Ph.D.

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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HIH RM

Identifier Type: -

Identifier Source: org_study_id

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