NCT04048044

CompletedPhase 1

EFFECTS OF RejuvaMatrix ™ ON TELOMERES

Holos Institutes of Health, Inc Source

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Other study identifiers

Sponsor study identifier

HIH RM

Study Type

interventional

Actual enrollment (reported)

50

Locations

0 countries

Sites

N/A

Timeline

Study Start

January 2009

Actual (reported)

Primary Completion

December 2014

Actual (reported)

Study Completion

December 2014

Actual (reported)

Brief Summary

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

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 50 participants
Study completion date: December 2014
Actual (reported)
Listed locations: 0 countries · 0 sites

Trial Relationships

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Some registry-reported names shown below are not yet linked in this graph.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
January 2009
Actual (reported)
First Submitted
May 10, 2012
Actual (reported)
Primary Completion
December 2014
Actual (reported)
Study Completion
December 2014
Actual (reported)
First Posted
August 7, 2019
Actual (reported)

Last Updated: August 7, 2019
Status Verified: May 2012
Last Update Submitted: August 6, 2019

Conditions

Telomeres

Outcome Measures

Primary Outcomes (1)

Length of telomeres after 5 years compared with baseline
5 years

Secondary Outcomes (1)

Total Symptom Index
5 years

Study Arms (1)

Telomere length, GigaHz exposure

ACTIVE COMPARATOR

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

Device: Exposure to GHz electromagnetic energy (RejuvaMatrix)

Interventions

Exposure to GHz electromagnetic energy (RejuvaMatrix)Device

75 decibels of 54 to 78 GHz daily for 60 minutes

Telomere length, GigaHz exposure

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age18 Years+

Sexall

Healthy VolunteersYes

Age GroupsAdult (18-64), Older Adult (65+)

You may not qualify if:

Implanted electronic device
Major, debilitating disease

Sponsors & Collaborators

Holos Institutes of Health, Inc
Otherlead

Enrollment

50 participants (actual enrollment reported by the registry).

Study Design

Study Type: interventional
Phase: phase 1
Allocation: NON RANDOMIZED
Masking: NONE
Purpose: SUPPORTIVE CARE
Intervention Model: SINGLE GROUP
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: M.D., Ph.D.

Study Record Dates

First Submitted

May 10, 2012

First Posted

August 7, 2019

Study Start

January 2009

Actual (reported)

Person living with an individual who has an implanted device

Person who is or could become pregnant

Contact the study team to confirm eligibility.

Primary Completion

December 2014

Actual (reported)

Study Completion

December 2014

Actual (reported)

Last Updated

August 7, 2019

Record last verified: 2012-05

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT04048044
Data provider: ClinicalTrials.gov
Source updated: 2019-08-07
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:30:49 UTC

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

Primary Completion

Study Completion

First Posted

Conditions

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (1)

Study Arms (1)

Telomere length, GigaHz exposure

Interventions

Eligibility Criteria

You may not qualify if:

Sponsors & Collaborators

Enrollment

Study Design

Study Record Dates

Source record