Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID04048993

Registry-based Biobank Development and Integrative Physiological Analysis

Led by University of Copenhagen · Updated on 2025-02-10

400

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are developing a registry-based biobank to support integrative physiological analysis by collecting biological samples such as blood, urine, interstitial fluid, adipose tissue, and muscle from participants. The study uses advanced data-mining and multivariate approaches that incorporate clinical and demographic information to better understand human physiology. This research is observational and aims to create a valuable resource for future scientific investigations. Participants enrolled in the Section registry will provide the biological samples needed for the biobank. The study involves gathering these samples alongside collecting clinical and demographic data to perform integrative analyses. No experimental treatments or interventions are administered; instead, the focus is on sample collection and data integration over an extended period. During the study, participants will undergo fatiguing exercise to qualify for inclusion, and their samples will be collected for analysis. Researchers will monitor the biobank's development over approximately five years, focusing on creating a comprehensive collection of physiological data and samples. The study allows healthy volunteers aged 18 and older to participate, with ongoing observation and data gathering to support future research.

CONDITIONS

Brief Title

Registry-based Biobank Development and Integrative Physiological Analysis

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Able to perform fatiguing exercise
Not Eligible

You will not qualify if you...

  • 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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Sample Collection

Duration - Up to 5 years

Participants provide biological samples including blood, urine, interstitial fluid, adipose tissue, and muscle for biobank development and integrysiological analysis.

Trial Site Locations

Total: 1 location

1

University of Copenhagen

Copenhagen, Denmark, 2100

Actively Recruiting

Loading map...

Research Team

M

Morten Hostrup, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here