RecruitingPhase 4ACTRN12607000567426

A open label, phase IV clinical trial examining the efficacy of Prothrombinex alone verses Prothrombinex combined with fresh frozen plasma in patients who require Warfarin reversal.

An open label, phase IV clinical trial examining the efficacy of Prothrombinex-VF alone verses Prothrombinex-VF combined with fresh frozen plasma in patients who require Warfarin reversal.


Sponsor

Frankston Hospital

Enrollment

40 participants

Start Date

Jan 1, 2008

Study Type

Interventional

Conditions

Summary

Study Title An open label, phase IV clinical trial examining the efficacy of Prothrombinex alone versus Prothrombinex combined with fresh frozen plasma in patients who require Warfarin reversal Trial Objectives The primary aim of this study is to determine whether Prothrombinex alone is adequate and effective in the reversal of the anticoagulant activity of Warfarin. Number of patients 40 Inclusion Criteria 1. Patients who are on Warfarin therapy with an asymptomatic INR >9 where the treating clinician wishes to reverse the effects of the drug 2. Any clinically significant bleeding where Warfarin induced coagulopathy is considered a contributing factor and an INR of >2.5 where Warfarin reversal is considered important by the clinician 3. Pre surgery if INR >2.5 on the day of surgery and the clinician requires reversal of the effects of Warfarin 4. Patient is = 18 years of age. 5. Patients that are able to understand and apply with study protocol requirements and instructions and intends to complete the study as planned.6. Patient signs and dates written informed consent. Exclusion Criteria 1. Active bleeding requiring blood transfusion. 2. Patients with a known allergy to prothrombin complex concentrates or fresh frozen plasma. 3. Participation in another pharmacotherapeutic study within 30 days. Objective criteria for study entry 1. Asymptomatic INR > 9 where there is a high risk of bleeding 2. Any clinically significant bleeding where Warfarin induced coagulopathy is considered a contributing factor and an INR >2.5 where Warfarin reversal is considered important by the clinician 3. Pre surgery if INR > 2.5 on day of surgery and the clinician requires reversal of the effects of Warfarin Outcomes The primary outcome is the rapid reversal of Warfarin as indicated by the correction of the INR to < 2. Safety outcomes: Allergic reaction to Prothrombinex, the development of a complicating thrombosis (venous or arterial) and the presentation of clinically overt bleeding


Eligibility

Sex: Both males and femalesMin Age: 18 YearssMax Age: 0 N/As

Plain Language Summary

Simplified for easier understanding

This study is comparing two approaches to reversing the blood-thinning effects of Warfarin (an anticoagulant medication). Warfarin is commonly used to prevent dangerous blood clots, but sometimes it needs to be reversed quickly — for example, before surgery or if the level gets dangerously high. One standard approach is to give a product called Prothrombinex along with fresh frozen plasma (FFP). This study is testing whether Prothrombinex alone is just as effective without needing the plasma component. You may be eligible if: - You are 18 years of age or older - You are currently taking Warfarin - Your INR (a blood clotting test) is greater than 9 and you have no symptoms of bleeding, OR you have clinically significant bleeding with an INR greater than 2.5, OR you are about to have surgery and your INR is above 2.5 You may NOT be eligible if: - You are actively bleeding and need a blood transfusion - You have a known allergy to prothrombin complex concentrates or fresh frozen plasma - You have participated in another drug study within the last 30 days Talk to your doctor about whether this trial might be right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

The subject will receive Prothrombinex-50units/kg body weight as an intravenous infusion.

The subject will receive Prothrombinex-50units/kg body weight as an intravenous infusion.


Locations(1)

Australia

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ACTRN12607000567426