Quality of Life in Patients With Double Loop Ureteral Stent (JJ Silicone Hydrogel Study)

Effect of a Silicone Hydrocoated Double Loop Ureteral Stent on Symptoms and Quality of Life in Patients Undergoing F-URS for Kidney Stone; a Comparative Randomized Multicenter Clinical Study.

This study is a prospective, randomized multicenter study conducted in Europe. It is designed to compare two double loop ureteral stents in terms of the quality of life in patients operated on a kidney stone and requiring the placement of a double loop ureteral stent at the end of the operation.

The double loop stents are used for both prevention and treatment of ureteral obstruction: They permit the interim internal bypass drainage of urine when obstruction in the ureter especially in cases of lithiasis or after surgical intervention on the upper urinary tract. There are many indications for double loop stent placement and population chosen for this study are adult patients with intra-renal calcium calculi of 7-20 mm in diameter for whom the treatment indication is a flexible ureterorenoscopy. The aims of the use of a double loop stent are to prevent complications (pain, infection) associated with the ureteral obstruction by any residual stone fragments, blood clot or local oedema generated by the intervention. preserve the renal function. facilitate healing process while limiting the risk of stenosis and probably reduce the rate of readmission after patients' discharge. Double loop Stent-related symptoms have a high prevalence and may affect over 80% of patients. Assessment tools are important to determine the symptoms intensity and allow for comparisons at different times. The Urinary Stent Symptom Questionnaire (USSQ) is the most adapted tool designed for this purpose. An ideal ureteral stent is expected to drain well, to be easy to insert and to be comfortable for the patients. The investigators designed a hydro-coated Silicone JJ stent with additional properties for improving patient's comfort. The investigators decided to perform a randomized clinical investigation to evaluate the Coloplast Hydrocoated Silicone JJ in comparison to the Boston Percuflex Plus JJ stent on patients' comfort.

A JJ stent placement may be indicated at the end of the endourological removal of kidney stones to ensure urine drainage and cicatrisation

Evaluate impact on quality of life via the USSQ questionnaire assessing 5 other scores and adverse event reporting at all visits.

Encrustation of double loop ureteral stents is evaluated by a score of integer values ranging from 0 to 6

Inclusion Criteria: Male and female patients Aged > 18 years Unilateral renal non-infection stone for whom the treatment indication is a flexible ureterorenoscopy (multiple kidney stones are acceptable provided that only one side is currently symptomatic) Index stone of 5-25 mm (measured on plain abdomen X-Ray KUB or CT) Without any currently implanted JJ stent Patient agreed to participate to the study and having signed the consent form Able to complete self-rated questionnaires. Exclusion Criteria: Acute ureteric/nephritic colic (residual pain is acceptable) Any type of chronic pain Large stones > 25 mm Infection renal stone already diagnosed and documented Malformation of urinary tract (e.g. Horseshoe kidney, duplicity or, ureterocele, mega ureter) Diverticulum stone Urogenital tumor Any significant neurological disease or injury impacting sensation JJ stents already implanted Patients with long-term indwelling urethral catheter No indication for JJ insertion (e.g. spontaneous stone passage) Untreated urinary tract infection Ureteral obstruction (stenosis, compression, calculi) Neurogenic bladder Overactive bladder Bladder stone Chronic prostatitis BPH treated (recent initiation of 5 alpha-Reductase Inhibitor or Phytotherapeutic agents) Ongoing Alpha-Blocker or Anticholinergic medication Pregnancy Any event discovered during the endoscopy which is not compatible with the study design and objective