CClinicalTrials.gg
Status unknownNCT01943981AF-CPXUpdated Sep 17, 2013

Exercise Performance in Patients With Atrial Fibrillation

An observational study in Atrial Fibrillation, sponsored by Incheon St.Mary's Hospital. Status unknown at 1 site in Korea, Republic of. Open to participants aged 30 Years to 80 Years. Per ClinicalTrials.gov, last updated 2013-09-17.

Sponsored by Incheon St.Mary's Hospital · Observational

The sponsor has not verified this record recently (last verified Sep 2013), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
50
Ages
30 Years to 80 Years
Sex
All
01

Study summary

Heart failure and stroke are the two major complication of atrial fibrillation. Current treatment for atrial fibrillation is so focused to stroke prevention, but the risk assessment for heart failure is less highlighted. The most of patients with atrial fibrillation have cardiac functional limitation of variable degree. We hypothesize that the exercise test would reveal the subclinical cardiac dysfunction, and might be helpful to classify the patients with atrial fibrillation according to their exercise capacity real cardiac function.

02

Conditions studied

  • Atrial Fibrillation

Browse trials for

03

In context

Atrial Fibrillation

3,870 studies on the registry are indexed under Atrial Fibrillation; 924 are open to participants now.

This study's planned enrollment of 50 is below the median of 300 across 1,363 observational studies indexed under Atrial Fibrillation.

Browse Atrial Fibrillation studies →

Lead sponsor

Incheon St.Mary's Hospital is the lead sponsor of 18 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
30 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with atrial fibrillation and preserved left ventricular systolic function

Inclusion criteria

  • Nonvalvular chronic atrial fibrillation
  • Left ventricular ejection fraction >40%

Exclusion criteria

Exclusion Criteria:

  • Acute decompensated heart failure within 30 days
  • unstable hemodynamic status
  • Significant coronary artery disease
  • Any condition interfering sufficient exercise
  • Valvular stenosis or regurgitation of moderate or severe degree
  • Obstructive or restrictive lung disease of moderate or severe degree
  • Active malignancy
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
50 participants (estimated)
Target follow-up
2 Years
Patient registry
Yes

Groups and cohorts

  • Optimal/inappropriate exercise response
06

What researchers measure

Primary outcomes

  1. Exercise response patterns of heart rate and oxygen uptake

    Time frame: At baseline

Secondary outcomes

  1. Composite cardiovascular events (all death, admission of heart failure, stroke/thromboembolism)

    Time frame: Up to 2 years

07

Study locations

1 site
  • Incheon St.Mary's Hospital
    Incheon, 403-720, Korea, Republic of
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 17, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01943981
Lead sponsor
Incheon St.Mary's Hospital
Responsible party
Mi-Jeong Kim (Assistant professor, Incheon St.Mary's Hospital) — Principal investigator
First posted
Sep 17, 2013
Start date
Sep 2013
Primary completion
Feb 2015 (estimated)
Last update
Sep 17, 2013

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2013. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion