A clinical trial to study the symptoms produced by a ureteral stent which is placed post surgery for stone disease.
Not Applicable
- Conditions
- Health Condition 1: N209- Urinary calculus, unspecified
- Registration Number
- CTRI/2023/02/049759
- Lead Sponsor
- Pushpanjali Hospital and Research Centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with stone disease.
Patients undergoing unilateral stenting.
Exclusion Criteria
Patients with any neurological condition
Patients with urinary tract malignancy
Patients with congenital urinary tract abnormality
Patients with comorbid urologic anatomical abnormalities, such as ureteral stricture
Pregnant or lactating females
Patients with known psychiatric illness
Patients who refused consent to participate in study
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the prevalence and bother of various urinary tract symptoms caused by indwelling ureteral stents using validated questionnaireTimepoint: Patients symptoms will be assessed at time of stent removal approximately 4 weeks after endourological procedure.
- Secondary Outcome Measures
Name Time Method Overall incidence of various stent related symptoms in patients undergoing endourological treatment for stone disease. <br/ ><br>Comparison of incidence of stent related symptoms with respect to different stent materials used. <br/ ><br>Comparison of incidence of stent related symptoms with respect to different sizes of the stent used. <br/ ><br>Impact of duration of stent, medication used and various other factors on ureteral stent related symptoms.Timepoint: Outcomes will be assessed after the removal of stent