- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04412928
Factors Affecting the Cure of Overactive Bladder Syndrome in Women Underwent Mid-urethral Sling Procedure
September 14, 2023 updated by: Sheng-Mou Hsiao, Far Eastern Memorial Hospital
We will estimate the incidence of patients with overactive bladder syndrome after surgery and explore related predictors.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
At present, around 30% of women with stress urinary incontinence have overactive bladder syndrome after mid-urethral sling procedure.
But its predictive factor is still unclear.
We will estimate the incidence of patients with overactive bladder syndrome after surgery and explore related predictors.
In addition, we will explore the cure rate and predictors of cure of overactive bladder syndrome after the mid-urethral sling procedure for women with stress urinary incontinence.
The above results will be used as a reference for preoperative and postoperative consultation.
Study Type
Observational
Enrollment (Actual)
591
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
-
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New Taipei
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Banqiao, New Taipei, Taiwan, 22050
- Department of Obstetrics and Gynecology, Far-Eastern Memorial Hospital
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-
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
20 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
All women with stress urinary incontinence who underwent mid-urethral sling procedure.
Description
Inclusion Criteria:
- All women with stress urinary incontinence who underwent mid-urethral sling procedure from January 01, 2008 to July 31, 2019 will be reviewed.
Exclusion Criteria:
- Patients undergoing other gynecological operations at the same time, except for cystoscopy.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Factors affecting the presence of overactive bladder syndrome after mid-urethral sling procedure
Time Frame: 10 year
|
10 year
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Factors affecting cure of overactive bladder syndrome after mid-urethral sling procedure
Time Frame: 10 years
|
10 years
|
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)
April 13, 2020
Primary Completion (Actual)
March 12, 2021
Study Completion (Actual)
April 20, 2021
Study Registration Dates
First Submitted
May 31, 2020
First Submitted That Met QC Criteria
May 31, 2020
First Posted (Actual)
June 2, 2020
Study Record Updates
Last Update Posted (Actual)
September 15, 2023
Last Update Submitted That Met QC Criteria
September 14, 2023
Last Verified
September 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Urologic Diseases
- Urinary Bladder Diseases
- Lower Urinary Tract Symptoms
- Urological Manifestations
- Urination Disorders
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Urogenital Diseases
- Male Urogenital Diseases
- Urinary Bladder, Overactive
- Urinary Incontinence
- Urinary Incontinence, Stress
Other Study ID Numbers
- 109048-E
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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