Calculation of Platelet-rich Plasma Preparation Yield

NCT ID: NCT03161743

Last Updated: 2017-08-10

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Total Enrollment

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-06-30

Study Completion Date

2018-05-31

Brief Summary

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This is a study to determine 1) the consistency of platelet-rich plasma produced by several methods, and 2) whether the platelet content of platelet-rich plasma can be accurately estimated from a baseline CBC platelet count.

Detailed Description

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In the first phase of this 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 platelet count will be measured in each PRP preparation and compared to the CBC platelet count to determine the platelet yield for each method.

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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Platelet-rich Plasma Production

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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venipuncture

blood draw for the purpose of determining the platelet concentration in PRP

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* English speaking

Exclusion Criteria

* platelet count \< 150,000
* platelet count \> 350,000
* History of blood disorder
* History of altered platelet function
* History of chemotherapy or radiation therapy
Minimum Eligible Age

21 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Harrison, Theodore, M.D.

INDIV

Sponsor Role lead

Responsible Party

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Theodore Harrison, MD

Principal Investigator

Responsibility Role 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

Site Status

Countries

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Canada

Other Identifiers

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PRP Platelet Yield

Identifier Type: -

Identifier Source: org_study_id

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