This prospective randomized controlled trial investigates the effects of alfuzosin, mirabegron, and their combination on stent-related symptoms and outcomes in patients undergoing DJ stent placement after retrograde intrarenal surgery (RIRS) for renal stones. The primary outcomes include stone-free rate and residual fragment status, while secondary outcomes focus on stent-related pain and lower urinary tract symptoms (LUTS). Patients will be randomly assigned to one of four groups: alfuzosin only, mirabegron only, combination therapy, or control. Pain and LUTS will be assessed using validated questionnaires such as the Ureteral Stent Symptom Questionnaire (USSQ) and IPSS.
Retrograde intrarenal surgery (RIRS) is a commonly used minimally invasive procedure for the treatment of renal stones. Postoperative placement of double-J (DJ) stents is often necessary but can result in significant stent-related discomfort and lower urinary tract symptoms (LUTS), which negatively impact patient quality of life. Alfuzosin, an alpha-blocker, and mirabegron, a beta-3 agonist, are pharmacological agents known to reduce stent-related symptoms. This study aims to compare the individual and combined efficacy of these agents on stent-related pain, LUTS, and postoperative stone outcomes. Patients will be evaluated for stone clearance, residual fragments (by imaging), and symptom scores over a follow-up period of 2 to 4 weeks post-RIRS
Study Type
OBSERVATIONAL
Enrollment
100
Gaziantep University Faculty of Medicine Hospital
Gaziantep, Turkey (Türkiye)
Stent-Related Pain Score
Pain score ranges from 0 to 39 (higher scores indicate worse pain).
Time frame: Day 7 postoperatively and Day 14 postoperatively.
Lower Urinary Tract Symptom (LUTS) Score
IPSS ranges from 0 to 35 (higher scores indicate more severe LUTS).
Time frame: Day 7 postoperatively and Day 14 postoperatively
Stone-Free Rate
Proportion of patients with no residual fragments \> 2 mm on NCCT
Time frame: Day 14 postoperatively
Residual Fragment Status
Categorization of residual fragments into 0 mm, 1-2 mm, or \> 2 mm
Time frame: Day 14 postoperatively
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