NCT05687578

Brief Summary

This is a minimal risk, prospective, non-randomized, multi-center population based observational study to establish a physical baseline profile for individual study subjects using various modalities (blood draws, non-invasive imaging, stool samples, saliva samples) and identify deviations through longitudinal monitoring that may develop over time and may be relevant to human health and healthy longevity.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
10,000

participants targeted

Target at P75+ for all trials

Timeline
44mo left

Started Mar 2023

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress46%
Mar 2023Jan 2030

First Submitted

Initial submission to the registry

January 3, 2023

Completed
15 days until next milestone

First Posted

Study publicly available on registry

January 18, 2023

Completed
2 months until next milestone

Study Start

First participant enrolled

March 27, 2023

Completed
5.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2029

Expected
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2030

Last Updated

October 15, 2024

Status Verified

October 1, 2024

Enrollment Period

5.8 years

First QC Date

January 3, 2023

Last Update Submit

October 9, 2024

Conditions

Aging

Keywords

Aging

Outcome Measures

Primary Outcomes (1)

  • Biomarkers that exhibit significant change

    The number of biomarkers that exhibit significant change from baseline to any follow-up timepoint, if obtained.

    12 Months

Interventions

Measurements OnlyDIAGNOSTIC_TEST

This is an observational study only using biospecimen and imaging-based measurements only

Eligibility Criteria

Age18 Years - 90 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

This is a prospective, population-based observational study. Participants may be recruited from clinical sites that are actively participating in the PUER Research comprehensive evaluation model. Participants and all participating health care providers are unblinded.

You may qualify if:

  • Male or non-pregnant female; age 18 to 90
  • Absence or presence of any medical history or any signs or symptoms of any disease
  • Women of childbearing potential (WOCBP) must have a negative urine pregnancy test (UPT) at all visits

You may not qualify if:

  • Unwillingness or inability to participate in the study
  • Unwillingness or inability to provide written Informed Consent Form
  • WOCBP with positive pregnancy test at enrollment or at any visit

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Puer Research, LLC

Atlanta, Georgia, 30350, United States

Location

Related Publications (28)

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Biospecimen

Retention: SAMPLES WITH DNA

Blood samples, including genomic samples

Study Officials

  • Szilard Voros, MD

    Puer Life

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
NETWORK
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 3, 2023

First Posted

January 18, 2023

Study Start

March 27, 2023

Primary Completion (Estimated)

January 1, 2029

Study Completion (Estimated)

January 1, 2030

Last Updated

October 15, 2024

Record last verified: 2024-10

Locations

US(1)