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Recruiting NCT04048993

Registry-based Biobank Development and Integrative Physiological Analysis

— Observational Integrative Human Physiology

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
The protocol lists: Biobank development and integrative physiological analysis.
Who it may be relevant to
Registry conditions: Integrative Human Physiology. Basic parameters: from 18 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
Denmark
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The purpose is to develop a registry-based biobank for integrative physiological analysis based on biological samples (blood, urine, interstitial fluid and muscle) from subjects enrolled in the Section registry, using multivariate and data-mining approaches that includes also clinical and demographic parameters

Interventions

  • Other Biobank development and integrative physiological analysis
    Collection of biological samples (blood, urine, interstitial fluid, adipose tissue and muscle) from subjects enrolled in the Section registry, using multivariate and data-mining approaches that includes also clinical and demographic parameters.

Primary outcome measures

  • Biobank creation [Time frame: through study completion, an average of 5 years]

Eligibility criteria

Inclusion criteria

  • able to perform fatiguing exercise

Exclusion criteria

  • severe mental or physical handicap
  • chronic disease deemed by the M.D. to preclude inclusion
  • use of prescription medicine deemed by the M.D. to preclude inclusion

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

Denmark · 1 center
  • University of Copenhagen — Copenhagen

Identifiers

NCT: NCT04048993 · BIO

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗