The standardisation of terminology in lower urinary tract function: report from the standardisation sub-committee of the International Continence Society.
Paul Abrams, Linda Cardozo, Magnus Fall...
https://pubmed.ncbi.nlm.nih.gov/12559262/Actively Recruiting
Led by Mackay Medical College · Updated on 2025-09-05
200
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are evaluating the bladders voiding function response after surgery with midurethral slings, such as the trans-obturator tape TOT, in women diagnosed with stress urinary incontinence SUI. The study aims to clarify whether the bladders thermodynamic efficiency changes following the TOT procedure, which is known for its effective cure rate and less invasive approach. Participants undergo urodynamic investigations including free uroflowmetry, postvoid residual measurements, filling and voiding cystometry, and urethral pressure profiles. These tests are conducted both before and 4-6 weeks after the TOT surgery, using saline at body temperature infused at a controlled rate. Data are analyzed to compare bladder function parameters such as maximum flow rate and detrusor pressure during voiding cycles. During the study, participants receive comprehensive urodynamic evaluations one to four weeks before surgery and again at a follow-up visit 4-6 weeks post-operation. The research team monitors various bladder function indicators and analyzes the pressure-volume relationship within voiding cycles to assess changes. This observational timeline helps determine the safety and efficacy of midurethral slings in improving bladder continence and function over time.
CONDITIONS
Efficacy/Safety of Midurethral Sling
H
Hui-Hsuan Lau, M.D.
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Mackay Medical College
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Pre-operative evaluation 1 to 4 weeks before surgery; post-operative evaluation at 4 to 6 weeks after surgery
Participants undergo a midurethral sling procedure for stress urinary incontinence and receive urodynamic evaluations before and after the operation.
2 visits (pre-operative and post-operative urodynamic evaluations, in-person)
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
34
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Lead Sponsor