Blood Specimen Collection For Laboratory Assay Research
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorRoman Health Ventures Inc.
About this trial
To collect lab data from capillary and venous blood specimens for use in analytical research studies to support the development and validation of laboratory procedures.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Any gender, in good general health
Must be 18 years old or older, inclusive at enrollment
Must be willing to provide capillary blood samples via a fingerstick and venous blood samples, including self-collection and collection by a licensed healthcare professional
Must be able to read, understand, and willingly sign an Informed Consent Form (ICF) and complete a brief health questionnaire
Disqualifiers
Individuals who are unable to provide a blood sample due to any illness
Individuals participating in another research study, that the Investigator feels may compromise study outcomes
Individuals having an acute or chronic disease or medical condition, including pregnancy, which could excessively increase study risk in the opinion of the Investigator or compromise study outcomes
Individuals who are unlikely to be available for the duration of the study
Trial population
Healthy members of the community aged 18 years and over
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
No trial groups listed
Trial outcomes
Primary outcomes
1
Correlation between capillary and venous samples upon collection
R-value comparing the lab readings generated by venous and capillary samples for a specific blood analyte immediately upon collection
Time frame
10 years2
Stability of the capillary blood sample after storage on Days 1, 2, and 3
Median error % to compare the difference in values of each capillary sample after storage for a certain period of time (e.g., Days 1, 2, and 3) for a specific analyte when compared to the lab reading generated by the venous sample immediately upon collection
Time frame
10 yearsSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov