NCT04062071

Brief Summary

Atrial fibrillation is a clinically significant cardiac arrhythmia that increases the risk of stroke by 3 to 4 times. Oral anticoagulation has been shown to mitigate stroke risk by two-thirds among patients with AF and is widely recommended in optimizing AF management.Direct oral anticoagulants have also been demonstrated to be superior to warfarin with respect to the risk of fatal bleeding and stroke prevention. However, the previous study finding highlighted a great gap between current guidelines and the clinical management of AF .Nonetheless, the decision for anticoagulant use is not straightforward.It is worth to investigate the updated prevalence of anticoagulant use, the reasons for not receiving anticoagulant, and the factors independently associated with anticoagulant refusal in patients with non-valvular atrial fibrillation.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
300

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Aug 2019

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 16, 2019

Completed
4 days until next milestone

First Posted

Study publicly available on registry

August 20, 2019

Completed
3 days until next milestone

Study Start

First participant enrolled

August 23, 2019

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 23, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 23, 2020

Completed
Last Updated

August 20, 2019

Status Verified

August 1, 2019

Enrollment Period

7 months

First QC Date

August 16, 2019

Last Update Submit

August 19, 2019

Conditions

Keywords

anticoagulants

Outcome Measures

Primary Outcomes (1)

  • The prevalence of anticoagulant use in non-valvular atrial fibrillation patients

    calculate the prevalence of anticoagulant use in non-valvular atrial fibrillation patients

    August 2019 to March 2020

Secondary Outcomes (1)

  • the rate of the refusal of anticoagulant use

    August 2019 to March 2020

Interventions

no intervention

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

all of the documented atrial fibrillation patients having regular follow up in GOPC in the study period

You may qualify if:

  • diagnosis as atrial fibrillation
  • aged ≧18 years
  • able to given consent

You may not qualify if:

  • Unable/unwillingness to sign informed consent to study
  • mechanical heart valve
  • moderate-to-severe mitral stenosis
  • Transient atrial fibrillation from reversible cause (e.g., during respiratory tract infection or bronchospasm)
  • pregnancy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

LIAO, Jiawei

Hong Kong, Hong Kong

Location

MeSH Terms

Conditions

Atrial Fibrillation

Condition Hierarchy (Ancestors)

Arrhythmias, CardiacHeart DiseasesCardiovascular DiseasesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
ECOLOGIC OR COMMUNITY
Time Perspective
CROSS SECTIONAL
Target Duration
2 Months
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
resident

Study Record Dates

First Submitted

August 16, 2019

First Posted

August 20, 2019

Study Start

August 23, 2019

Primary Completion

March 23, 2020

Study Completion

March 23, 2020

Last Updated

August 20, 2019

Record last verified: 2019-08

Data Sharing

IPD Sharing
Will not share

no Conflict of interest

Locations