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Cryoablation for Monomorphic Ventricular Tachycardia

← catalyst calendar

NCT05675865 · readout in 165 d

Sponsored by Adagio Medical (industry) · ADGM — their whole pipeline →.

Phase
Not applicable
Status
Active, not recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
206estimated
Sites
15
Countries
Canada, United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-09-11actualWhen the study began enrolling
Primary completion2027-01-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-03-30estimatedThe whole study's end, after follow-up
First posted2023-01-09actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-07actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Sustained VT

Intervention

  • Device: cryoablation procedure

Primary outcomes

what the primary-completion date above is the date OF
Primary Safety Endpoint for EFS and Pivotal phases is freedom from definite or probable device or procedure related Major Adverse Events (MAEs) that occur within 7 days following the cryoablation procedure.
measured 7 days following the ablation procedure
Primary Procedural Endpoint for EFS and Pivotal - Analysis of the proportion of subjects with non-inducible VT or no further ablation targets meeting the criteria for ablation at the end of the cryoablation procedure.
measured During Procedure
Primary Efficacy Endpoint for Pivotal Phase
measured 6 months after the procedure

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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