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Trial · NCT07898020

Registered outcomes20

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryPostoperative pain score6 hours after surgeryPain intensity measured with a 0-10 visual analog scale (VAS); 0 = no pain, 10 = worst imaginable pain.
SecondaryPostoperative pain scores1, 2 and 24 hours after surgeryPain intensity measured with a 0-10 visual analog scale (VAS); 0 = no pain, 10 = worst imaginable pain.
SecondaryNumber of rescue analgesic dosesFirst 24 hours after surgeryNumber of rescue analgesic doses administered in addition to the standardized postoperative analgesic regimen.
SecondaryMean intrarenal pressureIntraoperativeMean intrarenal pressure (mmHg) recorded continuously by the pressure-sensing flexible ureteroscope.
SecondaryMaximum intrarenal pressureIntraoperativeMaximum intrarenal pressure (mmHg) recorded during the procedure.
SecondaryTime with intrarenal pressure above 30 mmHgIntraoperativeTotal time (seconds) during which intrarenal pressure exceeds 30 mmHg.
SecondaryMean intrarenal fluid temperatureIntraoperativeMean intrarenal fluid temperature (degrees Celsius) recorded continuously with a temperature probe.
SecondaryMaximum intrarenal fluid temperatureIntraoperativeMaximum intrarenal fluid temperature (degrees Celsius) recorded during the procedure.
SecondaryTime with intrarenal fluid temperature above 43 degrees CelsiusIntraoperativeTotal time (seconds) during which intrarenal fluid temperature exceeds 43 degrees Celsius.
SecondaryIrrigation fluid volumeIntraoperativeTotal volume of irrigation fluid used (mL), measured by weighing saline bags.
SecondaryAspirated fluid volumeIntraoperativeVolume of fluid aspirated through the suction sheath (mL); applicable to the FANS group only.
SecondaryCollected outflow volumeIntraoperativeVolume of irrigation fluid collected in the fluid-collection drape (mL).
SecondaryRetained irrigation fluid volumeIntraoperativeIrrigation volume minus aspirated and collected volumes (mL).
SecondaryStone-free rateUp to 3 months after surgeryPercentage of participants without residual stone fragments on non-contrast computed tomography.
SecondaryPostoperative feverUp to 30 days after surgeryNumber of participants with body temperature of 38 degrees Celsius or higher.
SecondaryInfectious complicationsUp to 30 days after surgeryNumber of participants who develop systemic inflammatory response syndrome (SIRS) or urosepsis.
SecondaryPostoperative complicationsUp to 30 days after surgeryNumber of participants with any postoperative complication graded according to the Clavien-Dindo classification.
SecondaryUreteral wall injuryAt the end of the procedureGrade of ureteral wall injury according to the Post-Ureteroscopic Lesion Scale (PULS), assessed endoscopically.
SecondaryOperative timePerioperative/PeriproceduralTime from insertion of the semirigid ureteroscope to placement of the double-J stent (minutes).
SecondaryLength of hospital stayUp to 7 days after surgeryTime from surgery to hospital discharge (days).

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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