Fresh frozen plasma transfusion
BiologicalPre-procedure fresh frozen plasma transfusion (15 cc per Kg to a maximum of 5 units)
NCT Number: NCT02637427
The purpose of this study is to evaluate prophylactic fresh frozen plasma transfusion in patients with moderately elevated international normalized ratios (INR) prior to undergoing an invasive procedure.
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Notify Me21 year and older
All sexes
Interventional
Phase 3
Johns Hopkins University, The Johns Hopkins Hospital, Baltimore, Maryland, United States
Fresh frozen plasma is used very frequently in the US. Many plasma transfusions are given prior to a procedure in order to correct perceived bleeding risk, yet there is little evidence to support that use of plasma reduces bleeding. There has never been an adequately powered trial to establish the efficacy of plasma and document the risks. This pilot study will evaluate the feasibility of conducting a research protocol that will lead to a large scale clinical trial designed to evaluate the treatment effectiveness of prophylactic plasma transfusion in patients with moderately elevated INRs prior to undergoing an invasive procedure outside of the operating room.
Study subjects will be randomly allocated to either receive either plasma transfusion prior to the procedure, or to no treatment. Study outcomes will be compared between the two study arms. Recruitment rates, protocol adherence, and rates of study outcomes will be assessed to determine the feasibility of the large scale trial.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Pre-procedure fresh frozen plasma transfusion (15 cc per Kg to a maximum of 5 units)
Time frame: within 2 days post procedure
Change from pre-procedure hemoglobin to lowest within 2 days after procedure
Time frame: within 2 days post procedure
Differences in number of units of red blood cell transfusions between the two study arms
Time frame: within 2 days post procedure
Difference in rates between the two study arms
Time frame: with 2 days post procedure
Difference in rates between the two study arms
Time frame: with 2 days post procedure
2g/dL or greater fall in hemoglobin level
Time frame: day of procedure
Change from pre-procedure INR level
Time frame: day 1 post procedure
Change from pre-procedure INR level
Time frame: day 2 post procedure
Change from pre-procedure INR level
Time frame: in-hospital up to 7 days
Death
Time frame: within 2 days post procedure
Pneumonia or blood stream infection
Time frame: within 2 days post procedure
new admission to the intensive care unit
Rutgers, The State University of New Jersey
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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