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Break Wave(TM) Extracorporeal Lithotripter First-in-Human Study

A Study of the SonoMotion Break Wave(TM) System for the Comminution of Urinary Tract Stones

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03811171
Enrollment
70
Registered
2019-01-22
Start date
2019-08-20
Completion date
2027-03-30
Last updated
2025-07-29

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

Conditions

Renal Calculi, Urinary Calculi

Keywords

Stone, Lithotripsy, Calculi

Brief summary

This is a prospective, open-label, multi-center, single-arm (non-randomized) study to assess the safety and effectiveness of breaking stones in the upper urinary tract using the SonoMotion Break Wave technology. Up to 30 subjects will be included. The procedure will be performed in a hospital surgical environment as an outpatient (without being admitted) or in a non-surgical environment such as a clinic or office procedure room. The procedure will be performed under varying levels of anesthesia ranging from no anesthesia to general anesthesia (fully asleep). Stones will be limited to ≤ 10 mm for lower pole stones and ≤ 20 mm everywhere else. Safety will be measured by the self-reported occurrences of adverse events, unplanned emergency department or clinic visits, and the need for further intervention. Fragmentation will be measured by self-reported stone passage and a comparison of computed tomography (CT) images before and after the procedure.

Interventions

The Break Wave device will be used to exert a low amplitude burst of ultrasound waves focused at the kidney stone. The primary components of the device include an 85 mm aperture diameter therapy probe driven by a high voltage generator. The therapy probe has a cavity in the middle to accommodate coaxial alignment of an ultrasound imaging probe for treatment guidance.

Sponsors

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH
SonoMotion
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Individuals presenting with at least one kidney stone apparent on CT. * Stones must be within the upper urinary tract. * Stones are indicated for SWL treatment per the American Urology Association (AUA) 2016 guidelines.8 * Stones must be measured under CT to be within the AUA 2016 SWL guidelines (i.e. ≤ 10 mm for lower pole stones and ≤ 20 mm for non-lower pole stones).

Exclusion criteria

* Acute untreated urinary tract infection or urosepsis. * Uncorrected bleeding disorders or coagulopathies. * Pregnancy. * Uncorrected obstruction distal to the stone. * Patients receiving anticoagulants and who are unable or not willing to cease the medication for the Break Wave procedure. * Stones that are not echogenically visible or cannot be positioned within the Break Wave therapy focus. * Individuals belonging to a vulnerable group (pregnant, mentally disabled, prisoner, etc.). * Patients unwilling to comply with the follow-up protocol, including post-procedure CT. * Individuals under 18 years of age. * Anatomic presentations preventing adequate positioning or delivery of the Break Wave pulse. * Calcified abdominal aortic aneurysms or calcified renal artery aneurysms. * Solitary kidney * Comorbidity risks which, in at the discretion of the physician, would make the patient a poor candidate for the Break Wave procedure, such as anatomical anomalies that may not be conducive to adequate stone fragment passage.

Design outcomes

Primary

MeasureTime frameDescription
Primary Effectiveness Outcome - Stone Fragmentation12 weeks post-treatmentStone fragmentation as determined by stone passage or imaging confirmation.
Primary Safety Outcome - Hematoma, urinary tract sepsis, or cardiac arrythmia12 weeks post-treatmentThe documented occurrence of clinically significant or symptomatic hematoma (perirenal/intrarenal), urinary tract sepsis, or serious cardiac arrythmia.

Secondary

MeasureTime frameDescription
Secondary effectiveness outcome - Residual fragment size12 weeks post-treatmentPresence of only stone fragments small enough to pass (less than or equal to 4 mm).
Secondary safety outcome - Adverse events12 weeks post-treatmentdocumented occurrence of all adverse events and comparison of the incidence (rate of occurrence) to the adverse events associated with shock wave lithotripsy (SWL)
Secondary effectiveness outcome - Stone Free Status12 weeks post-treatmentRadiographic evidence (CT imaging) of stone free status.

Countries

Canada, United States

Contacts

Primary ContactOren Levy, PhD
oren.levy@sonomotion.com4156722631

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026