Study Of The Blood Thinner, Apixaban, For Patients Who Have An Abnormal Heart Rhythm (Atrial Fibrillation) And Expected To Have Treatment To Put Them Back Into A Normal Heart Rhythm (Cardioversion) (EMANATE)
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| ClinicalTrials.gov Identifier: NCT02100228 |
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Recruitment Status :
Completed
First Posted : March 31, 2014
Results First Posted : April 10, 2018
Last Update Posted : May 23, 2018
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Sponsor:
Pfizer
Collaborator:
Bristol-Myers Squibb
Information provided by (Responsible Party):
Pfizer
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Brief Summary:
Some people can develop an abnormal heart beat known as "Atrial fibrillation" or "AF" that puts them at risk of developing clots in the heart. Those clots can travel in the blood circulation to the brain and cause a brain attack ("a stroke"). To prevent those clots forming, blood thinners (anti-coagulants) are used. Apixaban is a blood thinner that works by stopping one of the blood substances required for clotting ("Factor Xa"). It is approved and used to prevent clots forming in people with "AF". Other established blood thinners work by stopping clotting substances being made, known as "Vitamin K antagonists" or "VKAs". An example of this type is Warfarin (Coumadin). The good effects of all blood thinners are preventing clots, and they may also have bad effects of increasing the chance of bleeding. People with "AF", abnormal heart beat, may benefit from changing it back to a normal regular rhythm, known medically as "cardioversion". When this is done, people are currently most commonly treated with a "VKA" blood thinner (e.g. warfarin). The purpose of this study is to assess the good and bad effects ("efficacy" and "safety") of apixaban compared with warfarin in people with "AF" in whom an early cardioversion is planned.
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Atrial Fibrillation | Drug: Apixaban Drug: Parenteral heparin and/or oral Vitamin K antagonist | Phase 4 |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 1500 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Supportive Care |
| Official Title: | A Phase Iv Trial To Assess The Effectiveness Of Apixaban Compared With Usual Care Anticoagulation In Subjects With Non-valvular Atrial Fibrillation Undergoing Cardioversion |
| Actual Study Start Date : | July 14, 2014 |
| Actual Primary Completion Date : | February 8, 2017 |
| Actual Study Completion Date : | February 8, 2017 |
Resource links provided by the National Library of Medicine
| Arm | Intervention/treatment |
|---|---|
| Experimental: Apixaban |
Drug: Apixaban
Oral, 2.5 or 5 mg BID |
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Active Comparator: Parenteral heparin and/or oral Vitamin K antagonist
Parenteral heparin and/or locally used oral Vitamin K antagonist e.g. warfarin (excludes other novel oral anticoagulants)
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Drug: Parenteral heparin and/or oral Vitamin K antagonist
Parenteral heparin and/or locally used oral Vitamin K antagonist e.g. warfarin (excludes other novel oral anticoagulants) |
Primary Outcome Measures :
- Number of Participants With Acute Stroke Event [ Time Frame: Baseline up to 30 days post cardioversion (or up to 90 days after randomization, if cardioversion was not performed within that time frame) ]An acute stroke was defined as a new, important neurological insufficiency of rapid onset that lasted for at least 24 hours and that was not due to a readily identifiable non-vascular cause (like brain tumor or trauma).
- Number of Participants With Systemic Embolism Event [ Time Frame: Baseline up to 30 days post cardioversion (or up to 90 days after randomization, if cardioversion was not performed within that time frame) ]Systemic embolism occurred in participant when there was a clinical history consistent with an acute loss of blood flow to a peripheral artery (or arteries), which was supported by evidence of embolism from surgical specimens, autopsy, angiography, or other objective testing.
- Number of Participants With Major Bleeding Event [ Time Frame: Baseline up to 30 days post cardioversion (or up to 90 days after randomization, if cardioversion was not performed within that time frame) ]Major bleeding was defined as clinically evident bleeding that was accompanied by one or more of the following: a decrease in hemoglobin of 2 gram per deciliter or more, a transfusion of 2 or more units of packed red blood cells, bleeding that was fatal or bleeding that occurred in at least one of the following critical sites: intracranial, intra-spinal, intraocular (within the corpus of the eye; thus, a conjunctival bleed was not an intraocular bleed), pericardial, intra-articular, intramuscular with compartment syndrome, retroperitoneal.
- Number of Participants With Clinically Relevant Non-Major Bleeding Events [ Time Frame: Baseline up to 30 days post cardioversion (or up to 90 days after randomization, if cardioversion was not performed within that time frame) ]Clinically relevant non-major bleeding was defined as the clinically evident bleeding that consisted of any bleeding that compromised hemodynamics, that led to hospitalization, subcutaneous hematoma larger than 25/100 centimeter square if there was a traumatic cause, intramuscular hematoma documented by ultrasonography, epistaxis, gingival bleeding occurred spontaneously, hematuria that was macroscopic and was spontaneous, macroscopic gastrointestinal hemorrhage included at least one episode of melena or hematemesis, rectal blood loss, hemoptysis or any other bleeding type considered to have clinical consequences for a participant, such as medical intervention, the need for unscheduled contact with a physician, or temporary cessation of a study drug, or associated with pain or impairment of activities of daily life.
- Number of Participants With All Cause Death [ Time Frame: Baseline up to 30 days post cardioversion (or up to 90 days after randomization, if cardioversion was not performed within that time frame) ]
Secondary Outcome Measures :
- Time to First Attempt of Cardioversion [ Time Frame: Baseline up to Day of first attempt of cardioversion procedure (Visit 2, up to 130 days) ]Cardioversion was an effective method of converting an abnormally fast heart rate (tachycardia) or other cardiac arrhythmia to normal rhythm using electricity or drugs. First attempt of cardioversion was defined as the first time the participant was admitted for the cardioversion procedure.
- Number of Participants With Different Type of Cardioversion Events [ Time Frame: Baseline up to Day of first attempt of cardioversion procedure (Visit 2, up to 130 days) ]Cardioversion was an effective method of converting an abnormally fast heart rate (tachycardia) or other cardiac arrhythmia to normal rhythm using different type of cardioversion events i.e. electrical and pharmacologic. Electrical cardioversion was a procedure in which an electric current was used to reset the heart's rhythm back to its regular pattern (normal sinus rhythm). Pharmacologic cardioversion, also called chemical cardioversion, used antiarrhythmia medication instead of an electrical shock.
- Number of Cardioversion Attempt of Participants [ Time Frame: Baseline up to Day of first attempt of cardioversion procedure (Visit 2, up to 130 days) ]Cardioversion attempts were defined as the number of times the participant was admitted to hospital for the cardioversion procedure and not the number of attempts during a single hospital admission.
- Number of Participants With Their Rhythm Status [ Time Frame: Baseline up to Day of first attempt of cardioversion procedure (Visit 2, up to 130 days) ]Rhythm status was further distinguished into sinus rhythm, atrial fibrillation and atrial flutter. Sinus rhythm was defined as a normal heartbeat. Atrial fibrillation was an irregular heartbeat (arrhythmia) that can lead to blood clots, stroke, heart failure and other heart-related complications and atrial flutter was a common abnormal heart rhythm that was usually associated with a fast heart rate (100 or more heart beats per minute).
- Duration of Hospital Stay of Participants [ Time Frame: Baseline up to Day of first attempt of cardioversion procedure (Visit 2, up to 130 days) ]Duration of hospital stay was defined as the number of hours from hospital admission to hospital discharge followed by early cardioversion.
- Number of Participants Who Used Image Guidance Approach [ Time Frame: Baseline up to Day of first attempt of cardioversion procedure (Visit 2, up to 130 days) ]An image-guided approach helped cardioversion earlier than the conventional minimum of 3 weeks of anticoagulation that would normally be required prior to cardioversion. Transesophageal echocardiography (TEE or TOE) and computed tomography (CT) were 2 image-guided approaches that were used in this study.
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| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Subjects with non-valvular atrial fibrillation (as documented by electrocardiogram (ECG) at Visit 1) indicated for cardioversion and initiation of anticoagulation in accordance with the approved local label. Subjects presenting with atrial flutter with no evidence of atrial fibrillation are not eligible for enrolment.
- Age ≥18 years (Age ≥ 19 years for Korea only and Age ≥ 20 years for Japan only).
- Evidence of a personally signed and dated informed consent document indicating that the subject (or their legally-recognized representative) has been informed of all pertinent aspects of the study.
- The subject is willing to provide contact details for at least one alternate person for study staff to contact regarding their whereabouts, should the subject be lost-to-follow-up over the course of the study. (Subject to IRB/IEC approval)
- Female subjects of childbearing potential must agree to use a highly effective method of contraception throughout the study and for at least 28 days after the last dose of assigned treatment. A subject is of childbearing potential if, in the opinion of the investigator, she is biologically capable of having children and is sexually active.
- Subjects who are willing and able to comply with scheduled visits, treatment plan, and other study procedures.
Exclusion Criteria:
- Subjects having taken more than 48 hours of an anticoagulant (oral and/or parenteral) immediately prior to randomization.
- Contraindications to apixaban or usual care (eg, VKA) in accordance with the approved local label.
- Severe haemodynamically compromised subjects requiring emergent cardioversion.
- Patients with hemodynamically significant mitral stenosis, mechanical or biological prosthetic valve or valve repair.
- Conditions other than atrial fibrillation that require chronic anticoagulation (eg, a prosthetic heart valve).
- Simultaneous treatment with both aspirin and a thienopyridine (eg, clopidogrel, ticlopidine, prasugrel) or simultaneous treatment with both aspirin and ticagrelor.
- Pregnant females; breastfeeding females; females of childbearing potential who are unwilling or unable to use a highly effective method of contraception as outlined in this protocol for the duration of the study and for at least 28 days after last dose of investigational product.
- Participation in other studies involving investigational drug(s) (Phases 1-4) within 30 days before the current study begins and/or during study participation. Note: Subjects cannot be randomized into this study more than once.
- Severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the subject inappropriate for entry into this study.
- Subjects who are investigational site staff members directly involved in the conduct of the trial and their family members, site staff members otherwise supervised by the Investigator, or subjects who are BMS/Pfizer employees directly involved in the conduct of the trial.
Information from the National Library of Medicine
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02100228
Locations
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Sponsors and Collaborators
Pfizer
Bristol-Myers Squibb
Investigators
| Study Director: | Pfizer CT.gov Call Center | Pfizer |
Study Documents (Full-Text)
Documents provided by Pfizer:
Documents provided by Pfizer:
Statistical Analysis Plan [PDF] February 2, 2017
Study Protocol [PDF] February 22, 2016
Additional Information:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Pfizer |
| ClinicalTrials.gov Identifier: | NCT02100228 |
| Other Study ID Numbers: |
B0661025 CV185-267 ( Other Identifier: Alias Study Number ) 2014-001231-36 ( EudraCT Number ) EMANATE ( Other Identifier: Alias Study Number ) |
| First Posted: | March 31, 2014 Key Record Dates |
| Results First Posted: | April 10, 2018 |
| Last Update Posted: | May 23, 2018 |
| Last Verified: | May 2018 |
Keywords provided by Pfizer:
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apixaban oral anticoagulant non-valvular atrial fibrillation cardioversion |
Additional relevant MeSH terms:
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Atrial Fibrillation Arrhythmias, Cardiac Heart Diseases Cardiovascular Diseases Pathologic Processes Vitamin K Heparin Apixaban Vitamins Micronutrients Physiological Effects of Drugs Anticoagulants |
Fibrinolytic Agents Fibrin Modulating Agents Molecular Mechanisms of Pharmacological Action Factor Xa Inhibitors Antithrombins Serine Proteinase Inhibitors Protease Inhibitors Enzyme Inhibitors Antifibrinolytic Agents Hemostatics Coagulants |