Effects of a 10 Component Dietary Supplement on Health and the Quality of Life
9. februar 2017 opdateret af: Centagen, Inc.
Effects of a Multi-Pathway Dietary Supplement (Stem Cell 100+) on Indices of Health and Life Expectancy
This open-label field trial evaluates the effects of treatment with a multi-pathway dietary supplement (Stem Cell 100+) that has been commercially available for several years.
The objective of the intervention trial is to determine if normal subjects over 35 years of age experience any observable health benefits from the dietary supplement as to their blood pressure, pulse rate, blood cholesterol, lung capacity, stress levels, or self reported changes in markers of overall health and life expectancy.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Currently, only dietary restriction has been verified to slow the rate of aging and to promote general health. This trial is designed to see whether a complex supplement (Stem Cell 100+) that targets multiple longevity pathways could also have positive effects on several markers of successful aging and good health. Multipath causes of aging include: stem cell function, telomere loss, chronic stress, inflammation, insulin-like growth factors, autophagy, vascular loss, neural dysfunction, and oxidative stress. The goal of the study was to test the effects of this novel multipath intervention strategy in a clinical trial of healthy people using health markers such as blood pressure, cholesterol status, lung function, stress levels, and self-reported health status. Hundreds of published animal and human clinical studies have been done with each of the individual active ingredients in the formulation, which target many critical causes of aging.
Based on their published animal studies showing extension of life span in a model animal and their laboratory work on adult human stem cells, the investigators believe that Stem Cell 100+ will provide evidence of efficacy in addressing multiple index markers of health and life expectancy outcomes.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
15
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
California
-
San Diego, California, Forenede Stater, 92121
- Accelagen, Inc.
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
35 år til 80 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- No history of serious cardiovascular, cancer, or neural disease.
- Normal health for age
- Willing to have blood drawn at baseline and after trial
- Willing to submit to evaluation testing of blood pressure, lung testing, stress testing.
- Willing to take online self reported survey of health at end of trial
Exclusion Criteria:
- History of metastatic cancer, heart attack, dementia, or other life-threatening disease
- Any subject who is not capable of responding to a self-reported online questionnaire
- Pregnant
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Stem Cell 100+ Intervention
Subjects take one 650 mg capsule by mouth twice daily for an average of 15 weeks
|
Open-Label 10-Component Dietary Supplement
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Blood Pressure
Tidsramme: Baseline and at an average of 15 weeks
|
Change in Systolic and Diastolic Blood Pressure
|
Baseline and at an average of 15 weeks
|
|
HDL Cholesterol
Tidsramme: Baseline and at an average of 15 weeks
|
Change in HDL Cholesterol
|
Baseline and at an average of 15 weeks
|
|
Lung Capacity
Tidsramme: Baseline and at an average of 15 weeks
|
Change in Peak Expiatory Flow
|
Baseline and at an average of 15 weeks
|
|
Stress Level
Tidsramme: Baseline and at an average of 15 weeks
|
Change in Heart Rate Variability
|
Baseline and at an average of 15 weeks
|
|
Heart Rate
Tidsramme: Baseline and at an average of 15 weeks
|
Change in Heart Rate
|
Baseline and at an average of 15 weeks
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Overall Health
Tidsramme: From baseline through study completion, an average of 15 weeks
|
Self-Reported Change based on a 7 point range from Much Better (+3) to Much Worse (-3)
|
From baseline through study completion, an average of 15 weeks
|
|
Ability to Concentrate or Focus
Tidsramme: From baseline through study completion, an average of 15 weeks
|
Self-Reported Change based on a 7 point range from Much Better (+3) to Much Worse (-3)
|
From baseline through study completion, an average of 15 weeks
|
|
Joint Flexibility
Tidsramme: From baseline through study completion, an average of 15 weeks
|
Self-Reported Change based on a 7 point range from Much Better (+3) to Much Worse (-3)
|
From baseline through study completion, an average of 15 weeks
|
|
Work Productivity
Tidsramme: From baseline through study completion, an average of 15 weeks
|
Self-Reported Change based on a 7 point range from Much Better (+3) to Much Worse (-3)
|
From baseline through study completion, an average of 15 weeks
|
|
Ability to Relax
Tidsramme: From baseline through study completion, an average of 15 weeks
|
Self-Reported Change based on a 7 point range from Much Better (+3) to Much Worse (-3)
|
From baseline through study completion, an average of 15 weeks
|
|
Cold/Flu Resistance
Tidsramme: From baseline through study completion, an average of 15 weeks
|
Self-Reported Change based on a 7 point range from Much Better (+3) to Much Worse (-3)
|
From baseline through study completion, an average of 15 weeks
|
|
Stress Tolerance
Tidsramme: From baseline through study completion, an average of 15 weeks
|
Self-Reported Change based on a 7 point range from Much Better (+3) to Much Worse (-3)
|
From baseline through study completion, an average of 15 weeks
|
|
Energy Level
Tidsramme: From baseline through study completion, an average of 15 weeks
|
Self-Reported Change based on a 7 point range from Much Better (+3) to Much Worse (-3)
|
From baseline through study completion, an average of 15 weeks
|
|
Endurance
Tidsramme: From baseline through study completion, an average of 15 weeks
|
Self-Reported Change based on a 7 point range from Much Better (+3) to Much Worse (-3)
|
From baseline through study completion, an average of 15 weeks
|
|
Ease of Walking
Tidsramme: From baseline through study completion, an average of 15 weeks
|
Self-Reported Change based on a 7 point range from Much Better (+3) to Much Worse (-3)
|
From baseline through study completion, an average of 15 weeks
|
|
Climbing Stairs
Tidsramme: From baseline through study completion, an average of 15 weeks
|
Self-Reported Change based on a 7 point range from Much Better (+3) to Much Worse (-3)
|
From baseline through study completion, an average of 15 weeks
|
|
Overall Mood
Tidsramme: From baseline through study completion, an average of 15 weeks
|
Self-Reported Change based on a 7 point range from Much Better (+3) to Much Worse (-3)
|
From baseline through study completion, an average of 15 weeks
|
|
Vitality
Tidsramme: From baseline through study completion, an average of 15 weeks
|
Self-Reported Change based on a 7 point range from Much Better (+3) to Much Worse (-3)
|
From baseline through study completion, an average of 15 weeks
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Ledende efterforsker: Bryant Villeponteau, Ph.D., Centagen, Inc.
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Generelle publikationer
- Villeponteau B, Matsagas K, Nobles AC, Rizza C, Horwitz M, Benford G, Mockett RJ. Herbal supplement extends life span under some environmental conditions and boosts stress resistance. PLoS One. 2015 Apr 16;10(4):e0119068. doi: 10.1371/journal.pone.0119068. eCollection 2015.
- Villeponteau B, Cockrell R, Feng J. Nutraceutical interventions may delay aging and the age-related diseases. Exp Gerontol. 2000 Dec;35(9-10):1405-17. doi: 10.1016/s0531-5565(00)00182-0.
- Villeponteau B. The heterochromatin loss model of aging. Exp Gerontol. 1997 Jul-Oct;32(4-5):383-94. doi: 10.1016/s0531-5565(96)00155-6.
- Marusic L, Anton M, Tidy A, Wang P, Villeponteau B, Bacchetti S. Reprogramming of telomerase by expression of mutant telomerase RNA template in human cells leads to altered telomeres that correlate with reduced cell viability. Mol Cell Biol. 1997 Nov;17(11):6394-401. doi: 10.1128/MCB.17.11.6394.
- Harley CB, Villeponteau B. Telomeres and telomerase in aging and cancer. Curr Opin Genet Dev. 1995 Apr;5(2):249-55. doi: 10.1016/0959-437x(95)80016-6.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
12. marts 2016
Primær færdiggørelse (Faktiske)
24. august 2016
Studieafslutning (Faktiske)
24. august 2016
Datoer for studieregistrering
Først indsendt
8. februar 2017
Først indsendt, der opfyldte QC-kriterier
9. februar 2017
Først opslået (Faktiske)
14. februar 2017
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
14. februar 2017
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
9. februar 2017
Sidst verificeret
1. februar 2017
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- SC100+ Clinical #1
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .