Clinical Trials Logo

Clinical Trial Summary

The aim of this study is to prospectively analyze patient satisfaction, pain, delivered energy and clinical effectiveness of using VR as a complimentary treatment modality during SWL.


Clinical Trial Description

The patients were randomized in two groups SWL with VR and SWL without VR. When a patient was randomized for a VR session we put on the monitor after adequate patient positioning. We used the Oncomfort Sedakit. The size and location of stone pre-treatment was measured based on the best available imaging tool (CT>RX/ultrasonography) using the maximal stone diameter. The locations of the stones were described as upper pole stones, midpolar stones, lower pole stones, renal pelvis stones and proximal ureteric stones. Each SWL treatment was standardized using diclofenac 100 mg suppository as analgesic and local lidocain/prilocain cream (EMLA 5g, Aspen) to numb the skin. Visualization of the stone was done by fluoroscopy of ultrasonography, as these proved to be equivalent (Van Besien et al. 2017). A specific and standardized ramping protocol was applied. After finishing this protocol, the energy level could be raised further depending on the level of discomfort of the patient. Directly after the procedure, the patients were asked to complete a questionnaire where they were asked to write down the experienced amount of pain during the procedure on a VAS of 10 cm and the satisfaction level using a Likert-scale. The total delivered energy was noted. Two weeks after every SWL session, follow-up imaging (ultrasound and plain abdominal radiography) was performed by a radiologist. Residual stone size was estimated on plain abdominal radiography or ultrasonography. The radiologist was blinded for the randomization process. Practitioner and patient were not. After each SWL the clinical outcome was noted. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05183269
Study type Interventional
Source AZ Sint-Lucas Gent
Contact
Status Completed
Phase N/A
Start date October 1, 2019
Completion date September 13, 2021

See also
  Status Clinical Trial Phase
Completed NCT05340075 - Staged Bilateral Percutaneous Nephrolithotomy
Completed NCT05340088 - Optimal Passive Dilation Time in Retrograde Intrarenal Surgery
Completed NCT05032287 - Medical Expulsive Therapy Post-SWL For Renal Stones N/A
Completed NCT06381206 - Silodosin in Management of Lower Ureteral Stones Phase 1/Phase 2
Completed NCT05646069 - Evaluation of Novel Disposable Flexible Ureteroscope for the Treatment of Renal Calculi N/A
Not yet recruiting NCT06436235 - Kidney Stone Inflammation
Completed NCT05413603 - Shock Wave Lithotripsy Using Fluoroscopic Versus Ultrasonic Localization N/A
Enrolling by invitation NCT06394908 - Registry of MIUS for Urolithiasis (ReMIUS-U)
Recruiting NCT05535816 - Accuracy of Ultrasound for Detecting Residual Fragments During RIRS N/A
Recruiting NCT05460559 - Endoscopic Combined Intrarenal Surgery Versus Multi-Tract Percutaneous Nephrolithotomy for Complex Renal Stones: N/A
Completed NCT03567421 - Ureteral Stenting After Ureteroscopy for Stone Treatment, A Global Perspective on Indications and Outcomes
Recruiting NCT05866081 - Stent Omission After Ureteroscopy and Lithotripsy in the Michigan Urological Surgery Improvement Collaborative N/A
Completed NCT04594161 - Effectiveness of Drainage by PCN vs. JJ in Patients With Symptoms of Obstructive Kidney Disease Caused by Urolithiasis N/A
Not yet recruiting NCT03771365 - Standard-PCNL vs Mini-PCNL vs Super-mini PCNL for the Treatment of ≥2 cm Renal Stone
Recruiting NCT04764071 - Ultra-Mini Versus Standard Percutaneous Nephrolithotomy For Management Of Renal Calculi. A Randomized Controlled Trial. Phase 3
Completed NCT06031103 - Clinical Efficacy of Mini-PCNLversus RIRS for the Management of Upper Urinary Tract Calculus (1-2.5 cm) N/A
Active, not recruiting NCT05759767 - The Efficacy and Safety of Medical Expulsive Therapy After Extracorporeal Shock Wave Lithotripsy (ESWL) in Pediatric Urolithiasis N/A
Not yet recruiting NCT04650737 - Single-Shot With Dexmedetomidine Versus Continuous Ultrasound-guided Erector Spinae Plane Block for Postoperative Pain Control After Percutaneous Nephrolithotomy N/A
Active, not recruiting NCT05389982 - Mobile Health Platform for Surveillance of Kidney Stone N/A
Completed NCT03388060 - (SWL) Versus (ODT) Versus Combined SWL And ODT For Radiolucent Stone N/A