- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07566741
A Prospective Analysis of Thulium Fiber Laser Efficiency
5. maj 2026 opdateret af: Volkan Selmi, Bozok University
A Prospective Analysis of Thulium Fiber Laser Efficiency: How Stone Volume and Density Predict Intraoperative Energy Consumption
Patients diagnosed with urolithiasis will be prospectively enrolled in this study.
Preoperative diagnostic assessment will be performed using computed tomography (CT).
Key parameters, including stone dimensions, quantity, total stone burden, and stone density (Hounsfield units), will be evaluated preoperatively.
This study aims to analyze data from patients who undergo ureteroscopic Thulium Fiber Laser (TFL) lithotripsy and achieve a stone-free status within a single procedural session.
Based on these data, a 'Specific Energy Coefficient' will be derived to enable the preoperative prediction of the total laser energy required for successful lithotripsy.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
This prospective observational trial investigated the correlation between Thulium Fiber Laser (TFL) energy consumption and stone characteristics.
Adult patients (≥18 years) with symptomatic urinary stones indicated for (f)URS and normal upper tract anatomy were included.
Only patients achieving a complete stone-free status in a single session were analyzed.
Exclusion criteria comprised active urinary tract infection, history of ipsilateral surgery or stent placement within six months, congenital renal anomalies, and postoperative residual fragments.
Stone parameters were evaluated via non-contrast computed tomography (NCCT, 1.0 mm slice thickness).
Mean stone density was measured in Hounsfield Units (HU) using a representative region of interest (ROI).
Stone volume (V) was calculated using the validated ellipsoid formula.
Procedures were performed by two high-volume endourologists using a 200 µm Thulium fiber.
Semirigid URS (7.5-9.5 F) or flexible URS (7.5 F) with an access sheath (10/12-12/14 F) were utilized based on stone location.
All cases employed "Dusting Mode" (0.1-0.2 J; 80-150 Hz).
Laser ablation time was recorded from the initial firing until complete visual stone clearance/dusting.
The primary outcome was the derivation of the Specific Energy Coefficient, calculated by dividing the total energy by the product of stone volume and density.
Data were analyzed using SPSS v26.0.
Normality was assessed via Shapiro-Wilk/Kolmogorov-Smirnov tests.
Descriptive data were reported as mean ± standard deviation or median.
Spearman's correlation and Multiple Linear Regression were used to identify independent predictors of laser energy requirements, with the model's predictive power reported as adjusted R2.
Statistical significance was set at p < 0.05.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
61
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
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Yozgat
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Yozgat, Yozgat, Tyrkiet (Türkiye), 66100
- Yozgat Bozok University Faculty of Medicine
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ingen
Beskrivelse
Inclusion Criteria:
- aged 18 years and above
- diagnosed with symptomatic urinary system stones
- planned URS or fURS
- normal upper urinary tract anatomy
- achieved stone-free
Exclusion Criteria:
- active urinary tract infection
- history of surgery/DJ stent placement within the last six months
- congenital renal anomalies
- patients with residual fragments on postoperative evaluation
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: Stone-free
|
Procedures were performed by two high-volume experienced endourologists.
Semirigid URS (7.5-9.5 F) was utilized for ureteral stones, while flexible URS (7.5 F) with a ureteral access sheath (10/12 F or 12/14 F) was preferred for renal stones.
A 200 µm Thulium fiber was employed in all cases.
Fragmentation was performed in Dusting Mode (Pulse Energy: 0.1-0.2
J, Frequency: 80-150 Hz).
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
thulium fiber laser energy consumption per mm3xHu
Tidsramme: 4 weeks
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4 weeks
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Ledende efterforsker: volkan selmi, Yozgat Bozok University
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
1. juni 2025
Primær færdiggørelse (Faktiske)
31. januar 2026
Studieafslutning (Faktiske)
31. januar 2026
Datoer for studieregistrering
Først indsendt
28. april 2026
Først indsendt, der opfyldte QC-kriterier
28. april 2026
Først opslået (Faktiske)
5. maj 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
8. maj 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
5. maj 2026
Sidst verificeret
1. maj 2026
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 2025-GOKAEK-2513
Plan for individuelle deltagerdata (IPD)
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Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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