- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04048993
Registry-based Biobank Development and Integrative Physiological Analysis
September 24, 2019 updated by: Morten Hostrup, PhD, University of Copenhagen
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
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
200
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Morten Hostrup, PhD
- Phone Number: 24474785
- Email: mhostrup@nexs.ku.dk
Study Locations
-
-
-
Copenhagen, Denmark, 2100
- Recruiting
- University of Copenhagen
-
Contact:
- Morten Hostrup, PhD
- Phone Number: 24474785
- Email: mhostrup@nexs.ku.dk
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Human subjects able to perform exercise
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Biobank creation
Time Frame: through study completion, an average of 5 years
|
Collection of biological samples from subjects included in the Section Registry
|
through study completion, an average of 5 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 1, 2019
Primary Completion (Anticipated)
August 10, 2024
Study Completion (Anticipated)
August 10, 2024
Study Registration Dates
First Submitted
August 5, 2019
First Submitted That Met QC Criteria
August 5, 2019
First Posted (Actual)
August 7, 2019
Study Record Updates
Last Update Posted (Actual)
September 25, 2019
Last Update Submitted That Met QC Criteria
September 24, 2019
Last Verified
September 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- BIO
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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