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NCT05845320 Clinical Trial

Prevalence of Stress Urinary Incontinence in Obese Versus Non-obese Nulligravid Women

Stress Urinary Incontinence Clinical Trial

Official title:
Prevalence of Stress Urinary Incontinence in Obese Versus Non-obese Nulligravid Women

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05845320
Other study ID # MS 188/2023
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 14, 2023
Est. completion date December 2023

Study information
Verified date May 2023
Source Ain Shams University
Contact Maii Nawara
Phone +201001848388
Email maii_nawara@hotmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Urinary incontinence (UI) is more common than any other chronic disease. Stress urinary incontinence (SUI), among the various forms of urinary incontinence, is the most prevalent (50%) type of this condition. Female urinary continence is maintained through an integrated function of pelvic floor muscles (PFMs), fascial structures, nerves, supporting ligaments, and the vagina. In women with SUI, the postural activity of the PFMs is delayed, and the balance ability is decreased. Many women, by learning the correct timing of a pelvic floor contraction during a cough, are able to eliminate consequent SUI. Timing is an important function of motor coordination and could be affected by proprioception. We aim to assess stress urinary incontinence in obese and non-obese Nulligravid females.

Recruitment information / eligibility
Status Recruiting
Enrollment 200
Est. completion date December 2023
Est. primary completion date December 2023
Accepts healthy volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Women aged between18 and 45 years. - Non obese females with BMI <25kg/m2. - Obese females with BMI =30kg/m2. - Nulligravid females. Exclusion Criteria: - Multiparous Females - Patients with active urinary tract infection. - Patients with respiratory or neurological diseases. - Patients with communication problems, cognitive disorders & mental disturbance. - Current treatment with drugs (benzodiazepines, diuretics) - Patients who underwent any previous abdominal or pelvic surgery.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• ICIQ-UI SF questionnaire
validated arabic short form of ICIQ on urinary incontinence

Locations
Country Name City State
Egypt Ain Shams University maternity hospital Cairo Cairo/???????

Sponsors (1)
Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Prevalence of Stress Urinary Incontinence in Obese Versus Non-obese Nulligravid Women as detected by questionnaire score 6 months
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