Actively Recruiting

Age: 50Years +
All Genders
Healthy Volunteers
NCT02604563

Aging, Geriatric Syndromes and Clonal Hematopoiesis

Led by Washington University School of Medicine · Updated on 2026-05-12

2000

Participants Needed

1

Research Sites

737 weeks

Total Duration

On this page

Sponsors

W

Washington University School of Medicine

Lead Sponsor

E

Edward P. Evans Foundation

Collaborating Sponsor

AI-Summary

What this Trial Is About

In this study the investigators will incorporate a wide range of clinical variables associated with aging and cardiovascular disease to determine whether they are associated with mutation status independent of chronologic age. Clinically, aging can be operationalized using geriatric assessment, which entails a comprehensive multi-dimensional assessment of the health of an older adult, including measures of comorbidity, polypharmacy, functional status, cognition, depression, falls, social activities and social support. Given that aging is heterogeneous, geriatric assessment allows greater specificity for aging than chronological age alone.

CONDITIONS

Official Title

Aging, Geriatric Syndromes and Clonal Hematopoiesis

Who Can Participate

Age: 50Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • At least 50 years of age.
  • Able to understand written and spoken English.
  • Able to understand and willing to sign an IRB-approved written informed consent document or that of a legally authorized representative if applicable for the trauma cohort.
Not Eligible

You will not qualify if you...

  • Unable or unwilling to complete health questionnaire except for hip replacement participants.
  • History of a recent acute viral illness within 30 days.
  • Current cancer diagnosis with ongoing chemotherapy or radiation therapy.
  • Current use of drugs causing DNA damage for non-cancer diseases.
  • Vulnerable populations such as prisoners.
  • Known infection with Hepatitis B or C, HTLV, or HIV.
  • For optional bone marrow biopsy: use of blood thinning medications or allergy to lidocaine or other local anesthetics.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Washington University School of Medicine

St Louis, Missouri, United States, 63110

Actively Recruiting

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Research Team

M

Meagan Jacoby, M.D.

CONTACT

K

Kristina Williams, B.S.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

5

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