Myocardial Infarction Clinical Trial
— Ripple-VTOfficial title:
Determining the Pathophysiological Role of Slow Conduction Channels Identified by Ripple Mapping of the Ventricular Scar.
NCT number | NCT02216760 |
Other study ID # | 14HH1922 |
Secondary ID | |
Status | Withdrawn |
Phase | N/A |
First received | |
Last updated | |
Start date | August 2014 |
Est. completion date | August 2018 |
Verified date | May 2019 |
Source | Imperial College London |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The heart beat is controlled by electrical signals. Following a heart attack, part of the
heart muscle dies and is later replaced by scar tissue. Within this area of scar, there often
remain "channels" of surviving tissue still able to transmit electrical signals. However, it
is well established that these "conduction channels" (CC) can form a short circuit around the
scar, leading to electrical disturbances (arrhythmias) that are potentially life threatening.
The commonest of these is ventricular tachycardia (VT), and is estimated to cause 300,000
deaths per year.
One recognised treatment option of VT involves burning (ablation) these "conduction channels"
(CC) within the scar. However, at present, the procedure is long and is far off 100%
effective. Consequently, current best practice does not rely on treating the VT, but rather
preventing it from causing sudden death - this is achieved with an Implantable Cardioverter
Defibrillator (ICD), a device which can recognise when a patient is in VT and deliver an
internal shock to restore the normal electrical conduction. Patients with defibrillators
subsequently are subject to recurrent painful and debilitating shocks which, although
lifesaving, significantly reduce their quality of life. The limitation with ablation at
present is due to the difficulty in visualising these CC's.
Investigators at Imperial College have created a novel electrogram visualisation program,
Ripple Mapping (RM), which they have already found to be superior to currently used
programmes in cases of arrhythmias in the upper chambers of the heart (the atria). During a
retrospective study in patients with scar related VT following a heart attack, when ablation
was delivered in areas associated with identified Ripple Mapping Conduction Channels, these
patients remained free of VT recurrence for >2 year follow up interval.
The study hypothesis is that Ripple Mapping can identify all conduction channels within scar
tissue critical to the VT circuit, ablation of which will lead to long-term freedom from VT
and ICD therapies. The investigators now aim to perform a prospective randomised study
comparing Ripple Mapping guided VT ablation against conventional VT ablation.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | August 2018 |
Est. primary completion date | August 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 85 Years |
Eligibility |
Inclusion Criteria: 1. Evidence of VT (shock/ anti tachycardia pacing/ detection) on ICD (single, dual or bi-ventricular) interrogation or 12 lead ECG. 2. Presumed scar related VT post myocardial infraction infarct/ dilated cardiomyopathy. 3. Age range 18-85yrs. 4. ICD implantation for primary or secondary prophylaxis, or device implantation pre-discharge from hospital post ablation procedure. 5. Signed informed consent Exclusion Criteria: 1. Contraindication to catheter ablation 2. Coronary revascularisation required 3. Ventricular tachycardia due to transient, reversible causes 4. Presence of cardiac thrombus 5. Severe cerebrovascular disease 6. Active gastrointestinal disease 7. Renal failure with creatinine >200 µmol/L or on dialysis 8. Active fever or infection 9. Life expectancy shorter than the trial 10. Allergy to contrast 11. Intractable heart failure (NYHA Class IV) 12. Bleeding or clotting disorders or inability to receive heparin 13. Pregnancy 14. Must not have previous (4 weeks prior to screening) or current participation in another clinical trial with an investigational drug or investigational device 15. Unable to give informed consent 16. Unable to attend follow-up visits or ICD clinics |
Country | Name | City | State |
---|---|---|---|
United Kingdom | Hammersmith Hospital, Imperial College Healthcare NHS Trust | London |
Lead Sponsor | Collaborator |
---|---|
Imperial College London |
United Kingdom,
Jamil-Copley S, Linton N, Koa-Wing M, Kojodjojo P, Lim PB, Malcolme-Lawes L, Whinnett Z, Wright I, Davies W, Peters N, Francis DP, Kanagaratnam P. Application of ripple mapping with an electroanatomic mapping system for diagnosis of atrial tachycardias. J Cardiovasc Electrophysiol. 2013 Dec;24(12):1361-9. doi: 10.1111/jce.12259. Epub 2013 Oct 10. — View Citation
Linton NW, Koa-Wing M, Francis DP, Kojodjojo P, Lim PB, Salukhe TV, Whinnett Z, Davies DW, Peters NS, O'Neill MD, Kanagaratnam P. Cardiac ripple mapping: a novel three-dimensional visualization method for use with electroanatomic mapping of cardiac arrhythmias. Heart Rhythm. 2009 Dec;6(12):1754-62. doi: 10.1016/j.hrthm.2009.08.038. Epub 2009 Sep 3. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Time to first appropriate ICD therapy | There will be a 1 week post procedural blanking period. Patients will be followed up at month 3, 6, 12, 18, 24 months for ICD device interrogation post blanking interval. The presence of appropriate ICD therapy as seen on the device download will be analysed on each occasion, and the time (days) from enrollment to the study to the ICD episode will be recorded. | 24 months post ablation procedure | |
Secondary | Total appropriate ICD episodes | There will be a 1 week post procedural blanking period. Patients will be followed up at month 3, 6, 12, 18, 24 months for ICD device interrogation post blanking interval. Appropriate ICD therapy burden (Anti-tachycardia Pacing + shocks) as well VT below the therapy zone will be recorded since the last device download and reset. The total number of episodes will be calculated and recorded for each patient at the end of 2 year follow up interval. | 24 months post ablation procedure | |
Secondary | VT induction post procedure | Immediately following VT ablation, programmed ventricular stimulation will be repeated to assess whether VT is inducible. Patient outcomes will be divided into 3 groups. Group A: VT non-inducible; Group B: Non-clinical VT induced. Group C: No RMCC's identified to guide ablation OR clinical VT remains inducible. The total number of patients in each group will be calculated and reported. | 1 day |
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