Menu
Recruiting NCT07305753

CanCan Body Composition Study

Observational Healthy Participants Young Healthy Adults Elderly (People Aged 65 or More)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Healthy Participants, Young Healthy Adults, Elderly (People Aged 65 or More). Basic parameters: 20 years — 90 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The aim of this study is to develop a dataset with reference body composition measurements using criterion methods. This dataset will be used to develop new protocols to study patients with cancer. Obtaining measurements of sodium bromide (NaBr), deuterium dilution (D2O), and D3-Creatine in a stratified sample of adults will determine the accuracy (and precision) of the available devices for ECW, TBW, and skeletal muscle mass measurements.

Primary outcome measures

  • Skeletal Muscle Mass [Time frame: Single time point]

Eligibility criteria

Inclusion criteria

  • Being either male or female
  • Being an adult >20 - <40 or >70 years of age.
  • Having a body weight of less than 440 pounds
  • Being willing to comply with the study procedures
  • Not having a chronic illness (e.g., diabetes, cancer, etc.)
  • Must be willing to have biospecimens and imaging stored for research use

Exclusion criteria

  • Being pregnant, attempting to become pregnant, or breastfeeding
  • Having medical implants such as a pacemaker or metal joint replacements
  • Having had a mastectomy, breast reduction, or breast implants
  • Having hair that cannot fit in a swim cap
  • Having a body weight greater than 440 pounds
  • Taking medications that alter the body's fluid compartments (ex: diuretics)
  • Not willing to have biospecimens and imaging stored for future research use.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

United States · 1 center
  • Pennington Biomedical Research Center — Baton Rouge

Identifiers

NCT: NCT07305753 · PBRC 00006218

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗