Actively Recruiting

Phase Not Applicable
Age: 19Years +
All Genders
NCT07411391

Supervised Endoscopic Tele-controlled Intelligent Lithotripsy

Led by Chinese University of Hong Kong · Updated on 2026-04-24

15

Participants Needed

1

Research Sites

58 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a phase I feasibility study to investigate the use of a novel intelligent robotic retrograde intrarenal surgery (RIRS) platform. The TaloStone T1000 RIRS system can manipulate the flexible ureteroscope, with remote control of the instruments (laser fibre or basket) and ureteral access sheath movements. Beyond teleoperation, the TaloStone T1000 RIRS system integrates AI perception models and decision-making algorithms to enable the supervised autonomous execution of critical tasks within the RIRS workflow.

CONDITIONS

Official Title

Supervised Endoscopic Tele-controlled Intelligent Lithotripsy

Who Can Participate

Age: 19Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients over 18 years old
  • Kidney stones less than 2 cm in maximum length
  • Clinically recommended for retrograde intrarenal surgery (RIRS)
  • Willing and able to give informed consent to participate
Not Eligible

You will not qualify if you...

  • No available preoperative CT imaging
  • Not recommended for RIRS by a doctor
  • Severe illness shortening life expectancy or increasing treatment risk
  • Untreated active infection
  • Uncorrected bleeding problems
  • Presence of another cancer or distant metastasis
  • Emergency surgery cases
  • Vulnerable individuals such as pregnant women or mentally disabled persons

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Prince of Wales Hospital

Hong Kong, Hong Kong, 999077

Actively Recruiting

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Research Team

A

Alex Qinyang Liu, MBBS, MSc, FRCSEd

CONTACT

C

Chi Fai Ng, MBChB, MD, FRCSEd

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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