ClinicalTrials.gg
RecruitingNCT07354347DAN-ATPUpdated Sep 4, 2026

Optimal Settings for Anti Tachycardia Pacing (ATP) on ICD

An interventional study of Burst and Ramp in Heart Disease, Implantable Cardioverter Defibrillator (ICD) and Heart Rhythm Disorders, sponsored by Rigshospitalet, Denmark. Recruiting at 1 site in Denmark. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-04.

Primary conditionTachycardia, VentricularRegistry: Heart DiseasesReclassifiedWhy we changed it
Registry
Heart Diseases — the first condition term the registry derived for this study.
ClinicalTrials.gg
Tachycardia, Ventricular
Why
  1. The study's listed conditions name Tachycardia, Ventricular, a narrower term within Heart Diseases.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Rigshospitalet, Denmark · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Feb 2026; still recruiting 9 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
3,980
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

This is a pragmatic, two-group, cluster randomized trial designed to compare strategies for the Anti Tachycardia Pacing (ATP)-setting in the ventricular tachyarrhythmias (VT) zone when implanting a new implantable cardioverter defibrillator (ICD) in patients with heart disease in hospitals in Denmark.

The strategies are: "Burst" or "Ramp" after 1. ATP (which is always burst) in VT zone. VT zone is defined between 180-249 (up to 269 in special cases) heartbeats per minute.

The ICD will give either:

Burst: The ICD is programmed to give ATP with 4 bursts. Or Ramp: The ICD is programmed to give ATP with 1 burst and 3 ramps.

The participating hospitals will be assigned to one of two intervention strategies for periods of 4-months. The given intervention will follow the patient/ICD throughout the life time of the ICD, but with the possibility to reprogram at any time (intention to treat).

It is calculated that the study needs a total of 398 events (second to fourth ATP), which is estimated to require 3980 implanted ICDs. The participants will be followed until the end of the ICD life, which is estimated to be around 10 years.

02

Conditions studied

  • Heart Disease
  • Implantable Cardioverter Defibrillator (ICD)
  • Heart Rhythm Disorders
  • Ventricular Tachyarrhythmias

Keywords

  • Heart failure
  • ICD
  • ATP
  • Anti Takykardi Pacing
  • Implantable Cardioverter Defibrillator
  • cluster randomisation
  • heart rhythm disorder
  • ventricular tachyarrhythmias
  • VT
03

In context

Tachycardia, Ventricular Reclassified

451 studies on the registry are indexed under Tachycardia, Ventricular; 120 are open to participants now.

This study's planned enrollment of 3,980 is above the median of 71 across 280 interventional studies indexed under Tachycardia, Ventricular.

Browse Tachycardia, Ventricular studies →

Lead sponsor

Rigshospitalet, Denmark is the lead sponsor of 1,007 studies on the registry; 175 are open to participants now.

Compared within Tachycardia, Ventricular, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Heart Diseases. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

- ICD implantation for primary or secondary prophylactic indication

Exclusion criteria

Exclusion Criteria:

  • None
  • Patients can actively opt out of participation in the study
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
3,980 participants (estimated)

Study arms

  • Experimental
    Burst

    Other: Burst

  • Experimental
    Ramp

    Other: Ramp

Interventions

  • OtherBurst

    ATP with 4 burst

  • OtherRamp

    ATP with 1 Burst + 3 Ramp

06

What researchers measure

Primary outcomes

  1. Arrhythmia cessation

    The ability of the given ATP protocol to stop the ventricular arrhythmia

    Time frame: The lifetime of the ICD, estimated 10 years

Secondary outcomes

  1. Defibrillation

    Arrhythmia accelerates resulting in defibrillation/shock therapy

    Time frame: The lifetime of the ICD, estimated 10 years

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No — The data are considered sensitive personal data.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 4, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07354347
Collaborators
The Novo Nordic Foundation
Responsible party
Bo Gregers Winkel (Chief Physician, Rigshospitalet, Denmark) — Principal investigator
First posted
Jan 21, 2026
Start date
Feb 1, 2026
Primary completion
Jul 31, 2041 (estimated)
Completion
Jul 31, 2041 (estimated)
Last update
Sep 4, 2026

Study contacts

Bo G Winkel, MD, PhD
Contact
bo.winkel@regionh.dk
+4535459759

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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