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NCT05535816 · ClinicalTrials.gov registry record · NA

Accuracy of Ultrasound for Detecting Residual Fragments During RIRS

A NA study, sponsored by University of California, San Francisco.

Terminated
Registry status
NA
Development phase
40
Enrollment target

NCT05535816: Clinical Trial NA study, sponsored by University of California, San Francisco.

NCT05535816 is a NA study that was terminated before completion, run by University of California, San Francisco. The registered enrollment target is 40 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05535816, a NA study, was terminated before completion, sponsored by University of California, San Francisco.

TERMINATED
Registry status
NA
Development phase
40 participants
Enrollment target

Study Summary

The purpose of this study is to assess the accuracy of ultrasound and traditional fluoroscopy to find the residual fragments before retrograde intrarenal surgery is complete. This would ultimately limit the need for radiation exposure and improve the quality of clinical care given to patients and healthcare teams.

Primary Outcome

The diagnostic accuracy of ultrasound and fluoroscopy will be measured in conjunction with endoscopic examination for detecting residual fragments during retrograde intrarenal surgery for renal stones treatment by the same endourologist to determine the size of the largest residual fragment, categorizing them as stone free, ≤ 2 mm, or \>2 mm, and compared with routine low-dose non-contrast computed tomography by a radiologist blinded to surgery and intraoperative imaging, categorizing them as st

Interventions

  • DIAGNOSTIC_TEST Ultrasound

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2023-03-27
Est. Completion 2024-12-18
Phase NA

Why NCT05535816 stopped before completion

NCT05535816 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 1 intervention - of which Ultrasound is the first listed.

NCT05535816 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05535816 about?

NCT05535816 is a clinical study titled "Accuracy of Ultrasound for Detecting Residual Fragments During RIRS". The purpose of this study is to assess the accuracy of ultrasound and traditional fluoroscopy to find the residual fragments before retrograde intrarenal surgery is complete. This would ultimately limit the need for radiation exposure and improve the quality of clinical care given to patients and he...

What is the current status of trial NCT05535816?

This trial is currently terminated. It is a NA study. The enrollment target is 40 participants. The study started on 2023-03-27. Estimated completion is 2024-12-18.

What interventions are being tested in trial NCT05535816?

The interventions under investigation include: Ultrasound (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT05535816?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05535816's enrollment target sits among peer trials

40 1447th of 2000 higher than 465 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05535816, the US trial registry maintained by the National Library of Medicine. NCT05535816 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.