MedPath

Effect of tamsulosin on reducing discomfort caused by ureteral stenting

Phase 2
Conditions
Discomfort after ureteral stenting in patients with urolithiasis.
Calculus of kidney and ureter
Registration Number
IRCT2015042221886N2
Lead Sponsor
Exir Pharmaceutical Company
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
70
Inclusion Criteria

age equal to 18 and more; urolithiasis indicated for transurethral litotripsy and Double J ureteral stenting thereafter.
Exclusion criteria: significant ureteral trauma; presence of previous ureteral stent; other concurrent operations; previous prostate resection; bladder tumors; urinary infections; history of chronic pain; pregnancy; age less than 18; prostate cancer; cardiovascular disease, coronary artery disease.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain interference with sleep. Timepoint: day 14 of intervention. Method of measurement: questionnaire.;Pain interference with daily activity. Timepoint: day 14 of intervention. Method of measurement: questionnaire.;Frequency of urination. Timepoint: day 14 of intervention. Method of measurement: questionnaire.;Flank pain. Timepoint: day 14 of intervention. Method of measurement: questionnaire.;Severity of pain during urination. Timepoint: day 14 of intervention. Method of measurement: questionnaire.;Painkiller consumption. Timepoint: day 14 of intervention. Method of measurement: questionnaire.
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath