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Clinical & Neurohormonal Prediction Of Outcome In Atrial Fibrillation

A study to assess whether clinical and neurohormal markers can predict the outcome of biphasic versus monsophasic cardioversion for atrial fibrillation.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12606000164594
Acronym
CHOP-CAF
Enrollment
280
Registered
2006-05-09
Start date
2003-01-08
Completion date
2009-10-23
Last updated
2024-09-30

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

Conditions

None listed

Brief summary

All patients on the waiting list for elective DC cardiovesion will be offered the chance to participate In this study. If they agree, we will record the results of the different laboratory and imaging tests that they had prior to presenting to the preadmission clinic, as well as each individual medical background. Each patient will have 4 extra blood tests to measure the hormones produced by the heart and other parts of the body in response to their heart condition. The first 2 tests will be on the day they present for the electric shock treatment (DC cardiovesion). The 3rd when having the 6 weeks routine follow up, and the last one will be when having the 6 months follow up. Each patient will, also, have an additional ultrasound examination of the heart 4-8 months following having the DC cardioversion. Each patient will be followed for a minimum of 1 year (the 2 other follow ups at 6&12 months post DC cardioversion). During this time we will monitor the heart rhythm, the rate of possible complications with this condition and analyse the data trying to identify the patients who may benefit from this treatment.

Interventions

Participants will also be randomly assigned to biphasic defibrillation as a single cardioversion procedure which takes about 3-5 minutes.

Sponsors

Christchurch Cardioendocrine Research Group
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Atrial fibrillation or flutter on the waiting list for elective DC cardioversion who are welling to participate and capable of attending follow up appointments.

Exclusion criteria

Any patient who is unable or not welling to consent to be enrolled, and patients who can not attend the follow up appointment.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026