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NCT01386892

Immunological Characterization of Blood of Normal Individuals

Completed Last updated 8 November 2021
What this trial tests

trial testing No intervention in Heathly Volunteers in 1,300 participants. Completed in 5 January 2015.

Timeline
1 March 2011
Primary endpoint
5 January 2015
5 January 2015

Quick facts

Lead sponsorOhio State University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment1,300
Start date1 March 2011
Primary completion5 January 2015
Estimated completion5 January 2015
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Ohio State University

Who can join

18 and older, any sex, with Heathly Volunteers. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study seeks to obtain normal samples of blood, saliva and urine to serve as controls for other approved protocols and for analysis. These include determination of the functional capabilities of cells, proteins, nucleic acids and microvesicles obtained from peripheral blood including plasma, serum and cellular fraction from normal individuals. Saliva and urine will have similar testing which may also be compared to the blood testing results. The ongoing objective varies from investigation to investigation but in general the investigational goals are to better understand the immune function of normal volunteers and compare it to immune function in disease states.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of No intervention

Trials testing the same drug.

Other Ohio State University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01386892.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing