Procedure For The Reference Range Study For Absolute MA
Completed
Conditions studied: Transmission, Blood, Recipient/Donor
In brief
CLSI guidelines shall be followed to gather data from a minimum of one hundred and twenty normal donors to create reference intervals for various Haemonetics reagents. Venous blood from a minimum of 146 reference subjects shall be tested. Blood from 160 donors will be drawn at the study site to account for aberrant or outlying data excluded for technical or other reasons.
Key facts
- Study ID
- NCT02110576
- Run by
- Haemonetics Corporation
- People needed
- 161
- Starts
- 2014-05-01
- Expected to finish
- 2015-03-01
- Last updated by the study team
- 2015-04-03
Who can join
Age: 18 and older, up to 85. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Male or Female over the age of 18 years.
- Self-identified as being in general good health, without chronic disease/illness, including but not limited to: cancer, diabetes mellitus, renal disease, cardiac disease, hypertension, lung disease, liver disease, complications of morbid obesity, autoimmune/inflammatory disease, or any condition of sufficient severity that it requires daily medication to manage
You may not qualify if…
- Age < 18 years.
- Infusion of blood products prior to the collection of blood samples.
- Known or subsequently discovered inherited defects of coagulation function (e.g. hemophilia or Von Willebrand's disease).
- Those females known to be pregnant
- Anticoagulant, antiplatelet, hormone or hormonal contraceptive therapy including aspirin use within the past month or NSAID use within the past week
- Surgery or traumatic injury within the previous 6 weeks
- Bruising, wounds or scarring in the area of venipuncture on the upper extremities
Where it is running
- Denver Health Medical Center — Denver, Colorado, United States
Full record on ClinicalTrials.gov
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