Cryoablation for Monomorphic Ventricular Tachycardia (VTS)

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NCT07650032 · readout in 224 d

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

Phase

Not applicable

Status

Recruiting

Study type

Interventional

Design

Na · None · Treatment

Enrollment

100estimated

Sites

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

Date

Filed

Basis

What it is

Start

2026-08-01

estimated

When the study began enrolling

Primary completion

2027-03-31

estimated

The date the last participant is measured for the primary outcome — the readout window

Study completion

2027-09-30

estimated

The whole study's end, after follow-up

First posted

2026-06-16

actual

When this record first appeared on the registry

Results posted

—

When the sponsor posted results to the registry

Record updated

2026-08-12

actual

The sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

Ventricular Tachycardia, Sustained
Ventricular Tachycardia, Monomorphic

Intervention

Device: Ultra Low Temperature Ablation (ULTA)

Primary outcomes

what the primary-completion date above is the date OF

Primary Safety Endpoint - Freedom from definite or probable device or procedure related Major Adverse Events (MAEs) that occur within 7 days following the ablation procedure.

measured 7 days following the ablation procedure

Primary Efficacy Endpoint - Freedom from recurrent sustained MMVT in the absence of a new AAD or increase in dose of a pre-ablation AAD for VT management at 6 months following the ablation procedure

measured 6 months after the procedure

Primary Procedural Endpoint - Percentage of non-inducibility VT targeted for ablation post-procedure

measured at the end of the ablation procedure

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