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The effectiveness of Detrositol and Omnic in reducing the discomfort caused by embedding the ureter stent

To compare the effectiveness of Detrositol and Omnic in reducing the discomfort caused by embedding the ureter stent with each other

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190624043991N13
Enrollment
150
Registered
2020-12-05
Start date
2019-12-01
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

Ureteral stone. Calculus of lower urinary tract

Interventions

Intervention 1: Intervention group: Patients receiving Omnic (Tamsulosin) 0.4 mg: 30 capsules: one daily, Cefixime 400 mg: 10 tablets: one daily and Naproxen 500 mg: 20 capsules: one every 12 hours af

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Patients candidates for Transurethral lithotripsy surgery for unilateral ureteral stones for the first time Age range 18-50 years Consent to participate in the study

Exclusion criteria

Exclusion criteria: No symptoms of BPH No history of any disease and treatment for prostatitis, cystitis and urinary symptoms No chronic side pain No history of ureteral stent placement in any of the ureters Not pregnant No history of urinary tract infection No history of chronic gastrointestinal pain No psychological illness, Malignancy No history of allergies or side effects of Tamsulosin and Tolterodine

Design outcomes

Primary

MeasureTime frame
Reduce complications from ureteral stents. Timepoint: The first day of surgery and one week after taking the medication, and before removing the stent. Method of measurement: Clinical Symptoms Questionnaire, Urine test and abdominal ultrasound.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Akram Mirzaei

Tehran University of Medical Sciences

mirzaee.scholar@gmail.com+98 21 6634 8560

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026