In Vitro Study of Platelets Collected on Trima Accel System and Stored in InterSol Solution
Completed · Not applicable
Conditions studied: Healthy Volunteers
In brief
This study sought to verify that the in vitro quality (functional assays) of platelets collected on the Trima Accel system, Version 6.4, diluted in InterSol Solution, and stored for 1, 5, and 7 days meet FDA requirements.
Key facts
- Study ID
- NCT02298842
- Run by
- Terumo BCT
- People needed
- 87
- Starts
- 2015-11-05
- Expected to finish
- 2016-05-12
- Last updated by the study team
- 2017-07-21
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Age 18 years of age or older
- Meet the inclusion criteria defined by the Investigational Site for an apheresis double platelet with plasma collection on the Trima Accel System. These criteria are based on American Association of Blood Banks (AABB) standards. Note: Subjects who are deferred from volunteer community donations because of travel restrictions, piercings or tattoos may participate in the study.
You may not qualify if…
- None.
Where it is running
- Hoxworth Blood Center — Cincinnati, Ohio, United States
- Blood Center of Wisconsin — Milwaukee, Wisconsin, United States
Full record on ClinicalTrials.gov
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