Monitor System for the Safety of Dabigatran Treatment

A Monitor System for the Safety of Dabigatran Anticoagulation Treatment in Nonvalvular Atrial Fibrillation

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02414035

Acronym

MISSION-AF

Enrollment

1496

Registered

2015-04-10

Start date

2015-03-22

Completion date

2018-04-18

Last updated

2019-09-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrial Fibrillation

Keywords

atrial fibrillation, anticoagulation, Dabigatran

Brief summary

The purpose of this study is to determine whether dabigatran is associated with higher risk of bleeding in Asia area especially in China clinical practice and whether it need to set up a monitor system.

Detailed description

Dabigatran is administered in a fixed does without laboratory monitoring and is being compared with warfarin (international normalized ratio, but only hundreds of evidence from Asia events in several multicenter, prospective, randomized trails. It remains unclear that whether Dabigatran is safety in China clinical practice and no need of monitor test. We identified participants as those diagnosed as having nonvalved atrial fibrillation, and who initiated dabigatran after diagnosis.We followed up each individual from the first prescription of dabigatran until discontinued use or switch of anticoagulants, death, or other outcomes or until one year later. We categorized bleeding events as major and minor events according to anatomical position. We defined time to bleeding as days between the first dabigatran prescription and the date of the bleeding event. We analyzed the time to the first bleeding event, as well as the time to the first major hemorrhage, intracranial hemorrhage, gastrointestinal bleeding, hematuria, vaginal bleeding, hemarthrosis, hemoptysis, and epistaxis.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

1. Age\>18 y at entry 2. AF documented as follows: The patients has a symptomatic episode of paroxysmal or persistent AF documented by 12-lead ECG, rhythm strip, pacemaker/implantable cardioverter-defibrillator electrogram, or Holter ECG 3. In addition to documented AF, patients must have ≥1 CHADS2-VAS scores 4. We identified participants as those diagnosed as having AF, and who initiated dabigatran after diagnosis 5. Written, informed consent

Exclusion criteria

1. History of heart valve disorders (ie, prosthetic valve or hemodynamically relevant valve disease) 2. Severe, disabling stroke, or any stroke within the previous 14d 3. Acute coronary syndrome within 1 year in AF patients 4. Conditions associated with an increased risk of bleeding 1. Major surgery in the previous month 2. History of intracranial, intraocular, spinal, retroperitoneal or atraumatic intra-articular bleeding 3. Gastrointestinal hemorrhage or hematuria 5. Severe renal impairment (estimated creatinine clearace≤30ml/min) 6. Severe liver dysfunction 7. Alcohol abuse or drug addiction 8. Patients who have received an investigational drug at this time 9. Patients considered unreliable by the investigator or have a life expectancy less than the expected duration of the trail

Design outcomes

Primary

Measure	Time frame	Description
Major bleeding events	up to 12 months (or) years	Any of the following events happened: intracranial hemorrhage, hemoperitoneum, and inpatient or emergency department stays for gastrointestinal, hematuria,or NOS hemorrhage
Minor bleeding events	up to 12 months (or) years	Any of the following events happened: epistaxis, hemoptysis, vaginal hemorrhage, hemarthrosis and any outpatient claim for hematuria, gastrointestinal, and NOS hemorrhage.

Countries

China

Outcome results