Ignite Creation Date:
2024-05-05 @ 11:43 PM
Last Modification Date:
2024-10-26 @ 10:38 AM
Study NCT ID:
NCT01391780
Status:
COMPLETED
Last Update Posted:
2013-12-11
First Post:
2011-07-08
Brief Title:
Pelvic Floor Muscle Evaluation in Women With Stress Urinary and Urgency Urinary Incontinence
Sponsor:
UPECLIN HC FM Botucatu Unesp
Organization:
UPECLIN HC FM Botucatu Unesp
Study Overview
Official Title:
Pelvic Floor Muscle Evaluation in Women With Stress Urinary and Urgency Urinary Incontinence A Prospective Trial
Status:
COMPLETED
Status Verified Date:
2011-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Aims To assess pelvic floor muscle PFM strength in women with stress urinary incontinence SUI and urgency urinary incontinence UUI
Methods 51 women were prospectively divided into two groups according to the symptoms as SUI G1 22 or UUI G2 29 Demographic data such as number of Pads 24 hours number of micturitions 24 hours and nocturia delay time of urgent void ie the time period for which an urgent void could be voluntarily postponed number of parity and vaginal deliveries were obtained using a clinical questionnaire Objective urine loss was evaluated by 60-min Pad Test Subjective urine stream interruption test UST visual survey of perineal contraction and transvaginal digital palpation and objective vaginal manometry evaluations of PFM were performed in all patients
Methods 51 women were prospectively divided into two groups according to the symptoms as SUI G1 22 or UUI G2 29 Demographic data such as number of Pads 24 hours number of micturitions 24 hours and nocturia delay time of urgent void ie the time period for which an urgent void could be voluntarily postponed number of parity and vaginal deliveries were obtained using a clinical questionnaire Objective urine loss was evaluated by 60-min Pad Test Subjective urine stream interruption test UST visual survey of perineal contraction and transvaginal digital palpation and objective vaginal manometry evaluations of PFM were performed in all patients
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None