Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
40 participants
OBSERVATIONAL
2017-06-30
2018-05-31
Brief Summary
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Detailed Description
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In the second phase of the study a baseline CBC platelet count will be performed on each subject and then platelet-rich plasma (PRP) prepared from the same blood sample by six different methods. The CBC platelet count will be used to calculate the estimated platelet content of each sample/method based on the platelet yields determined in the first phase. The platelet count will be measured in each PRP preparation and compared to the estimated platelet content to determine the predictive accuracy for each method.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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venipuncture
blood draw for the purpose of determining the platelet concentration in PRP
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* platelet count \> 350,000
* History of blood disorder
* History of altered platelet function
* History of chemotherapy or radiation therapy
21 Years
80 Years
ALL
Yes
Sponsors
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Harrison, Theodore, M.D.
INDIV
Responsible Party
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Theodore Harrison, MD
Principal Investigator
Principal Investigators
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Theodore E Harrison
Role: PRINCIPAL_INVESTIGATOR
Theodore Harrison
Locations
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Theodore E Harrison
Sidney, British Columbia, Canada
Countries
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Other Identifiers
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PRP Platelet Yield
Identifier Type: -
Identifier Source: org_study_id
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