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CompletedNCT02268799Updated Aug 13, 2015

High Sensitivity Troponin T Levels Following DC Cardioversion for Atrial Fibrillation / Atrial Flutter

An observational study in Atrial Fibrillation and Atrial Flutter, sponsored by University of Limerick. Completed at 1 site in Ireland. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2015-08-13.

Sponsored by University of Limerick · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
101
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to determine if there is a rise in serum high sensitivity troponin T (a marker for heart muscle injury) following a direct current cardioversion (shock therapy) used for patients with atrial fibrillation. This will help us determine if direct current cardioversion results in damage to the heart muscles in a sufficient amount to cause a rise in high sensitivity troponin T.

Read the detailed description

High sensitivity Troponin T is a relatively new biomarker that is highly sensitive and specific for myocardial injury. Its widespread use has helped in the determination and investigation for myocardial ischemia in patients. Previous studies have shown a rise in creatine kinase (CK) and the more specific creatine kinase-MB isoenzyme (CKMB) after DC cardioversion. Studies on the earlier generation troponin T found that the levels don't rise or rise only minimally after DC cardioversion. The high sensitivity troponin T has never been studied in the setting of DC cardioversion.

02

Conditions studied

  • Atrial Fibrillation
  • Atrial Flutter

Keywords

  • Cardioversion
  • High Sensitivity Troponin T (Hs-Trop T)
  • Brain Natriuretic Peptide (BNP)
  • Neutrophil Gelatinase-associated Lipocalin (NGAL)
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 enrollment of 101 is below the median of 300 across 1,363 observational studies indexed under Atrial Fibrillation.

Browse Atrial Fibrillation studies →

Lead sponsor

University of Limerick is the lead sponsor of 56 studies on the registry; 9 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with atrial fibrillation/flutter who attend the Coronary Care Unit of the University Hospital Limerick for a pre-organised appointment for direct current external cardioversion will be requested to participate in the study

Inclusion criteria

  • Patients with atrial fibrillation / atrial flutter attending for direct current external cardioversion
  • Age 18 or older

Exclusion criteria

Exclusion Criteria:

  • Myocardial infarction within the last 6 weeks
  • Coronary artery bypass grafting, percutaneous coronary intervention or any other invasive cardiac procedure within the last 6 weeks
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Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
101 participants (actual)
Patient registry
No

Groups and cohorts

  • DC Cardioversion

    Patients undergoing DC cardioversion

06

What researchers measure

Primary outcomes

  1. High Sensitivity Troponin T levels pre and 6 hours post cardioversion

    Time frame: 1 year

Secondary outcomes

  1. Creatine Kinase levels pre and 6 hours post cardioversion

    Time frame: 1 year

  2. B-type Natriuretic Peptide (BNP) levels pre and 6 hours post cardioversion

    Time frame: 1 year

  3. Neutrophil Gelatinase-associated Lipocalin (NGAL) levels pre and 6 hours post cardioversion

    Time frame: 1 year

07

Study locations

1 site
  • University Hospital Limerick
    Dooradoyle, Limerick, Ireland
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 13, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02268799
Lead sponsor
University of Limerick
Responsible party
Ronstan Lobo, MB, BMedSc, MRCPI, MRCP(UK) (Dr., University of Limerick) — Principal investigator
First posted
Oct 20, 2014
Start date
Oct 2014
Primary completion
Aug 2015
Completion
Aug 2015
Last update
Aug 13, 2015

Study contacts

Thomas J Kiernan, MD
study chair · University of Limerick

Oversight

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

Not currently enrolling

This study is completed, as verified in Aug 2015. You cannot join it, but the record below documents what was studied.

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