- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07447518
Double j Stent Related Symptoms
February 26, 2026 updated by: Elsayed Abdelhalim Elsayed, Kafrelsheikh University
Comparison of Mirabegron ,Tamsulosin and Solifenacinin Relieving Double -J Stent Related Symptoms : Approspective Randmized Placebo Controlledtrial
In urology, ureteral stents are used to treat obstructive diseases.
Hematuria (54%), fever, discomfort, and lower urinary system symptoms are the predominant symptoms related to ureteral stent.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
535
Phase
- Early Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Zagazig, Egypt, 44749
- Elsayed Abdelhalim
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- age above 18 years
- any patient need post urs or pcnl double stent
Exclusion Criteria:
- age less than 18 years
- known over active bladder patient
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Group A : patients will receive tadalafil
|
once daily 5mg
|
|
Active Comparator: Group B: patients will receive solidosin
|
once daily
|
|
Active Comparator: Group C: patients will receive solfenacin
|
once dialy
|
|
Active Comparator: Group D: patients will receive mirabegron
|
once daily
|
|
Placebo Comparator: Group E: patients will receive placebo
|
once daily
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Double j related symptoms
Time Frame: Six weeks
|
Double j related symptoms questionnaire score
|
Six weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sex matters related double j stent
Time Frame: Six weeks
|
Sex matters related stent
|
Six weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 22, 2022
Primary Completion (Actual)
January 1, 2023
Study Completion (Actual)
September 1, 2023
Study Registration Dates
First Submitted
January 17, 2025
First Submitted That Met QC Criteria
February 26, 2026
First Posted (Actual)
March 3, 2026
Study Record Updates
Last Update Posted (Actual)
March 3, 2026
Last Update Submitted That Met QC Criteria
February 26, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Urological Manifestations
- Pathological Conditions, Signs and Symptoms
- Signs and Symptoms
- Lower Urinary Tract Symptoms
- Pyridines
- Heterocyclic Compounds, 1-Ring
- Heterocyclic Compounds
- Heterocyclic Compounds, 2-Ring
- Heterocyclic Compounds, Fused-Ring
- Indoles
- Indole Alkaloids
- Heterocyclic Compounds, 3-Ring
- Carbolines
- Tadalafil
- mirabegron
Other Study ID Numbers
- 35806/9/22
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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