Actively Recruiting
High Versus Low Power Settings During Ureteroscopic Laser Lithotripsy
Led by Haukeland University Hospital · Updated on 2025-03-05
150
Participants Needed
1
Research Sites
140 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The primary aim of the study is to compare the operative times following ureteroscopic lithotripsy for renal stones with Thulium Fiber Laser using low and high power settings. Secondary aims are to compare the results of low and high power settings in terms of stone free rates, laser time, laser activation patterns, intraoperative and postoperative complications. Patients ≥ 18 years with renal stones (8-25 mm) scheduled for ureteroscopic lithotripsy at the Day Surgery Clinic at Haukeland University Hospital in Bergen, Norway, are eligible for inclusion in the study. After written consent and inclusion, patients are randomised to laser lithotripsy using either low power settings (Group 1: 4-6 Watt, short pulse mode) or high power settings (Group 2: 16-18 Watt, short pulse mode). The ureteroscopic procedures are performed in general anaesthesia using a standardised technique. All patients are followed up with a low dose CT scan 3 months post endoscopically to assess stone free status as well as a consultation at the outpatient clinic. Results and data for the two randomisation groups are compared according to the aims of the study.
CONDITIONS
Official Title
High Versus Low Power Settings During Ureteroscopic Laser Lithotripsy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients 18 years or older scheduled for ureteroscopic lithotripsy for renal stones sized 8-25 mm at Haukeland University Hospital day surgery unit
You will not qualify if you...
- Presence of a ureteral stone at the same time
- History of urinary diversion
- Active infection
- Untreated cancer in the upper urinary tract
AI-Screening
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Trial Site Locations
Total: 1 location
1
Haukeland University Hospital
Bergen, Vestland, Norway, 5021
Actively Recruiting
Research Team
Ø
Øyvind Ulvik, Assoc Prof
CONTACT
M
Mathias S Æsøy, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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