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临床试验/NCT03161743
NCT03161743Unknown不适用

Calculation of Platelet-rich Plasma Preparation Yield From Baseline CBC Platelet Count

Harrison, Theodore, M.D.1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2017年6月30日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
40
试验地点
1
主要终点
Platelet yield

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
21 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •English speaking

排除标准

  • •platelet count < 150,000
  • •platelet count > 350,000
  • •History of blood disorder
  • •History of altered platelet function
  • •History of chemotherapy or radiation therapy

结局指标

主要结局

Platelet yield

时间窗: within 8 hours of blood draw

the number of platelets in a PRP sample as a percentage of the number of platelets in the blood from which the PRP was prepared.

Platelet yield estimate accuracy

时间窗: within one month of final data collection

standard deviation of the difference between the estimated platelet yield and the actual platelet yield.

次要结局

未报告次要终点

研究者

发起方
Harrison, Theodore, M.D.
申办方类型
Indiv
责任方
Principal Investigator
主要研究者

Theodore Harrison, MD

Principal Investigator

Harrison, Theodore, M.D.

研究点 (1)

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