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Surgical Outcomes and Costs in Using the Shenzhen HugeMed 6.3 French Flexible Ureteroscope

Recruiting

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* Males or females ≥ 18 years of age
* Patients with ureteral or kidney stones undergoing primary flexible ureteroscopy for retrograde intrarenal surgery
* Total stone burden ≤ 2.5 cm

Exclusion Criteria:

* Undergoing bilateral stone treatment during the same procedure
* Patients with known genitourinary anatomical abnormalities that would complicate the procedure as determined by the treating investigator
* Uncorrected coagulopathy
* Patients with urinary diversions
* Chronic external urinary catheters
* Women who are pregnant
* Immunosuppressed patients
* Non-elective procedures
* Participants must not be involved in any other clinical research studies during the duration of this trial. Exceptions may be made if the investigator determines, on a case-by-case basis, that participation in another study will not adversely affect the outcomes or integrity of this trial

About the study

Comprehensive comparative investigations between HugeMed HU30M 6.3 Fr f-URS and traditional approach f-URS devices in RIRS are lacking in an American population. The investigators aim to compare the outcomes of using the 6.3 Fr f-URS versus traditional approach (other f-URS present in our institution) to treat patients with stone burden ≤ 2.5 cm. The findings of this study will expand on the potential advantages and drawbacks of HU30M in enhancing surgical outcomes and patient safety in RIRS procedures. We hypothesize that the use of the HU30M will result in increased cost savings while providing similar stone free rates when compared to traditionally used f-URS devices.

What is being tested

Sponsor: University of Kansas Medical Center · Participants: 75 · Started: May 1, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07296835

Locations in the U.S.

KansasUniversity Of Kansas Medical Center, Kansas City

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.