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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.

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02489656
Enrollment
140
Registered
2015-07-03
Start date
2013-09-30
Completion date
2016-12-31
Last updated
2015-07-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Kidney Calculi

Keywords

Double loop ureteral stent, USSQ, Quality of life, Pain

Brief summary

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.

Detailed description

* 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.

Interventions

DEVICEDouble Loop Ureteral stent endoscopic placement.

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

Sponsors

Coloplast A/S
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Male and female patients 2. Aged \> 18 years 3. 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) 4. Index stone of 5-25 mm (measured on plain abdomen X-Ray KUB or CT) 5. Without any currently implanted JJ stent 6. Patient agreed to participate to the study and having signed the consent form 7. Able to complete self-rated questionnaires.

Exclusion criteria

1. Acute ureteric/nephritic colic (residual pain is acceptable) 2. Any type of chronic pain 3. Large stones \> 25 mm 4. Infection renal stone already diagnosed and documented 5. Malformation of urinary tract (e.g. Horseshoe kidney, duplicity or, ureterocele, mega ureter) 6. Diverticulum stone 7. Urogenital tumor 8. Any significant neurological disease or injury impacting sensation 9. JJ stents already implanted 10. Patients with long-term indwelling urethral catheter 11. No indication for JJ insertion (e.g. spontaneous stone passage) 12. Untreated urinary tract infection 13. Ureteral obstruction (stenosis, compression, calculi) 14. Neurogenic bladder 15. Overactive bladder 16. Bladder stone 17. Chronic prostatitis 18. BPH treated (recent initiation of 5 alpha-Reductase Inhibitor or Phytotherapeutic agents) 19. Ongoing Alpha-Blocker or Anticholinergic medication 20. Pregnancy 21. Any event discovered during the endoscopy which is not compatible with the study design and objective

Design outcomes

Primary

MeasureTime frame
USSQ scale (Ureteral Stent Symptoms Questionnaire)at day 20

Secondary

MeasureTime frame
Evaluate impact on quality of life via the USSQ questionnaire assessing 5 other scores and adverse event reporting at all visits.Day 2, 7 and 35

Other

MeasureTime frameDescription
Encrustation of double loop ureteral stentsafter 20 days (JJ stent removal)Encrustation of double loop ureteral stents is evaluated by a score of integer values ranging from 0 to 6

Countries

France

Contacts

Primary ContactPascale HS Holliday, CTM
frpho@coloplast.com+33 1 40 83 68 58
Backup ContactDorothee Behr, Med Manager
frdbe@coloplast.com+33 1 40 83 68 50

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026