About this trial
Double-J ureteral stents are commonly inserted after ureteroscopy, but they may cause bothersome urinary symptoms, pain, sleep disturbance, and reduced quality of life.
This prospective randomized assessor-blinded three-arm clinical trial will compare oral solifenacin, oral melatonin, and their combination for improving ureteral stent-related symptoms in adult patients after unilateral ureteroscopic lithotripsy with insertion of a unilateral Double-J ureteral stent.
Participants will be randomized to receive solifenacin 5 mg once daily, melatonin 3 mg once nightly, or combined solifenacin 5 mg once daily plus melatonin 3 mg once nightly for 14 days after surgery. The primary outcome is the total Ureteral Stent Symptom Questionnaire score at postoperative Day 7. Secondary outcomes include total Ureteral Stent Symptom Questionnaire score at Day 14, change in questionnaire score between Day 7 and Day 14, Insomnia Severity Index score, Visual Analogue Scale pain score, adverse events, treatment compliance, and rescue analgesic consumption.
Eligibility criteria
Qualifiers
Age 18 to 60 years.
Patients undergoing unilateral ureteroscopy or ureteroscopic lithotripsy with insertion of a unilateral Double-J ureteral stent.
Ability to understand and complete the study questionnaires.
Willingness to participate and provide written informed consent.
Disqualifiers
Bilateral ureteral stents.
Stents inserted for malignant ureteral obstruction or non-stone reconstructive indications.
Known hypersensitivity or contraindication to solifenacin or melatonin.
History of acute or chronic urinary retention, or evidence of clinically significant bladder outlet obstruction at baseline.
Trial design
Treatments tested in this trial
- Solifenacin
- Melatonin