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Recruiting NCT06291441

NCT06291441 Women Urinary Incontinence Prevalence Study (WUIPS)

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Clinical Trial Summary
NCT ID NCT06291441
Status Recruiting
Phase
Sponsor IRCCS San Raffaele
Condition Female Urinary Incontinence
Study Type OBSERVATIONAL
Enrollment 449 participants
Start Date 2024-07-03
Primary Completion 2025-12-31

Eligibility & Interventions

Sex Female only
Min Age 40 Years
Max Age 65 Years
Study Type OBSERVATIONAL
Interventions
No intervention

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 449 participants in total. It began in 2024-07-03 with a primary completion date of 2025-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The goal of this multicenter prospective and prevalence observational study is to punctually investigate and describe prevalence, predictors, quality of life and costs of Urinary Incontinence (UI) among female patients, female caregivers and female personnel in four hospitals in Northern Italy: San Raffaele hospital in Milan, San Raffaele Turro hospital in Milan, Zingonia Policlinico San Marco (BG) and Policlinico San Pietro in Ponte San Pietro (BG).

Eligibility Criteria

INCLUSION CRITERIA * Female sex * Middle age (40-65 years old) * Informed consent signed * Comprehension of written and spoken Italian language * Female outpatients intended for any hospital unit (outpatient clinic, day surgery and day hospital patients included) and every female caregiver respecting the previous inclusion criteria, recruited at the central admission and at the private admission of the four hospitals involved * Female workers (healthcare professionals and administrative personnel) of the four hospitals EXCLUSION CRITERIA * Male sex * Young age (\< 40 years) and older age (\> 65 years) * Pregnant women * Puerperium women (up to 40 days post-partum) * Women who had undergone urinary and gynecology surgery

Contact & Investigator

Central Contact

Sara Trapani

✉ trapani.sara@hsr.it

📞 338 9879403

Principal Investigator

Duilio F. Manara

STUDY DIRECTOR

Director of Center for Nursing Research and Innovation (CeNRI)

Frequently Asked Questions

Who can join the NCT06291441 clinical trial?

This trial is open to female participants only, aged 40 Years or older, up to 65 Years, studying Female Urinary Incontinence. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06291441 currently recruiting?

Yes, NCT06291441 is actively recruiting participants. Contact the research team at trapani.sara@hsr.it for enrollment information.

Where is the NCT06291441 trial being conducted?

This trial is being conducted at Osio Sotto, Italy, Bergamo, Italy, Milan, Italy, Milan, Italy.

Who is sponsoring the NCT06291441 clinical trial?

NCT06291441 is sponsored by IRCCS San Raffaele. The principal investigator is Duilio F. Manara at Director of Center for Nursing Research and Innovation (CeNRI). The trial plans to enroll 449 participants.

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