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NCT Number: NCT07516106

Prospective Multi-center Study Comparing Pulsed Tm:YAG Laser to Pulse Modulated Holmium Laser in the Treatment of Nephrolithiasis With FANS Access Sheaths

The purpose of this study is to compare two laser technologies that are routinely used during ureteroscopy for the treatment of kidney stones. Specifically, this study will compare a pulsed Thulium:YAG laser to a pulse-modulated Holmium:YAG laser (Moses technology) to evaluate how effective and safe they are when used to break kidney stones.

Primary endpoints include stone-free rate and the zero stone-free rate at a standardized postoperative. Secondary endpoints include total operative time, lasing time (s), laser energy expended (J), efficiency (laser energy expended/stone volume; stone volume/lasing time). These endpoints aim to provide a comprehensive assessment of the clinical effectiveness and procedural efficiency of the two laser systems.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Mayo Clinic Arizona, Phoenix, Arizona, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Solitary renal stone 7 to 20 mm in size or in the case of multiple stones the conglomerate diameter (additive maximal diameter of all stones on axial imaging of computed tomography) of 7-20 mm is required
  • Must be a suitable operative candidate for flexible ureteroscopy per American Urological Association guidelines
  • Must be 18 years or older
  • Must be able to give consent
  • Bilateral ureteroscopy will be permitted , but only the side(s) where the FANS access sheath was used (per surgeon discretion) will be included in the study, however can include both sides as separate units. Subjects will be enrolled only once in the study. No subject will be enrolled more than a single time. For patients undergoing bilateral ureteroscopy, each kidney will be considered a separate unit for stone-related assessments. Peri-patient measures, such as operative time, will be recorded at the patient level. Bilateral cases will be clearly identified and handled consistently to ensure accurate and appropriate interpretation of study outcomes.
  • Must be a patient of one of the surgeons participating in this study.

Exclusion criteria

  • Concomitant stones in the ureter
  • Prior radiotherapy to the abdomen or pelvis
  • Neurogenic bladder or spinal cord injury
  • Pregnancy
  • Untreated urinary tract infection (UTI)
  • Anatomical abnormalities (including, but not limited to, bifid system, pelvic kidney, horseshoe kidney)
  • Prior ipsilateral upper urinary tract reconstructive procedures or history of ipsilateral ureteral stricture

Treatment and study plan

Moses Holmium:YAG laser

Device

Ho:YAG with Moses pulse modulation

Other names: MOSES 2.0 Technology

Thulium:YAG laser

Device

p-Tm:YAG laser lithotripsy with long pulse mode

Other names: Thulio

Primary outcomes

  1. Stone-free rate (absence of any fragments ≥ 2mm)

    Time frame: Month 1

  2. Zero stone-free rate (absence of any residual fragments confirmed by negative CT scan postoperative at one month)

    Time frame: Month 1

Secondary outcomes

  1. Total operative time

    Time frame: From first insertion of instruments to final removal of all instruments (up to 3 hours)

  2. Lasing time

    Time frame: From start of lasing to end of lasing (up to 1 hour)

  3. Laser energy expended (J)

    Time frame: From start of lasing to end of lasing (up to 1 hour)

  4. Laser energy expended per stone volume

    Time frame: From start of lasing to end of lasing (up to 1 hour)

  5. Stone volume per lasing time

    Time frame: From start of lasing to end of lasing (up to 1 hour)

Study contacts

Contact information is provided by the study sponsor or research team.

Esteban Emiliani, MD, PhD

CONTACT

[email protected]

646-290-4549

Rozalba Gogaj, MD, MPH

CONTACT

[email protected]

646-825-5663

Sponsors and collaborators

Lead sponsor

NYU Langone Health

Other

Registry information

Official study title

Prospective Multi-center Study Comparing Pulsed Tm:YAG Laser to Pulse Modulated Holmium Laser in the Treatment of Nephrolithiasis With Flexible And Navigable Ureteric Access Sheath (FANS)

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Apr 7, 2026
Registry last updated
Apr 7, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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