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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04121936
Other study ID # 1072.6120.160.2019
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 11, 2019
Est. completion date June 1, 2021

Study information

Verified date July 2022
Source Jagiellonian University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The first large population-based study to evaluate lower urinary tract symptoms (LUTS) in Poland. The study objective is to assess the prevalence and bother of LUTS in the population aged ≥40 years in Poland.


Description:

The first large population-based study to evaluate lower urinary tract symptoms (LUTS) in Poland. The study objective is to assess the prevalence and bother of LUTS in the population aged ≥40 years in Poland. This study will be conducted as a telephone survey with assessment of LUTS using a standardized protocol, which included the International Prostate Symptom Score (IPSS) and, for overactive bladder (OAB), the OAB-V8 questionnaire. Participants will be asked to rate how often they experienced individual LUTS and the degree of associated bother. The study will be performed in a representative group of Polish population (n = 6,000) covering all geographic regions of Poland (defined by the Central Statistical Office of Poland).


Recruitment information / eligibility

Status Completed
Enrollment 6000
Est. completion date June 1, 2021
Est. primary completion date December 31, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 40 Years to 100 Years
Eligibility Inclusion Criteria: Age >40 Exclusion Criteria: Age <40 Pregnancy Urinary tract infection in the past 4 weeks

Study Design


Related Conditions & MeSH terms


Intervention

Other:
There will be no intervention
There will be no intervention

Locations

Country Name City State
Poland Department of Urology Jagiellonian University Krakow

Sponsors (2)

Lead Sponsor Collaborator
Jagiellonian University Piotr Chlosta

Country where clinical trial is conducted

Poland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prevalence of LUTS The prevalence of LUTS will be assessed using definitions of the International Continence Society (descriptive statistics). Through study completion, an average of 3 months
Primary Symptom bother of LUTS The degree of associated bother will be assessed using Likert scale (Likert scale: not at all [score 0], a little bit [score 1], somewhat [score 2], quite a bit [score 3], a great deal [score 4], or a very great deal [score 5]). Through study completion, an average of 3 months
Secondary Prevalence of specific symptoms The prevalence of specific symptoms will be assessed using a standardised protocol based on the definitions provided by the International Continence Society (i.e. storage symptoms, voiding symptoms and post-micturition symptoms) [Abrams P, Cardozo L, Fall M, et al. The standardisation of terminology of lower urinary tract function: report from the Standardisation Sub-committee of the International Continence Society. Neurourol Urodyn. 2002;21:167-178]. Participants will be asked to rate how often they experienced individual LUTS during the past month. A Likert scale will be used with the following options: none (score 0), <1 in 5 times (score 1), Through study completion, an average of 3 months
Secondary Symptom bother of specific symptoms The degree of associated bother of specific symptoms will be assessed using Likert scale (Likert scale: not at all [score 0], a little bit [score 1], somewhat [score 2], quite a bit [score 3], a great deal [score 4], or a very great deal [score 5]). Through study completion, an average of 3 months
Secondary Prevalence of OAB The prevalence of OAB will be assessed with the Overactive Bladder-Validated 8-question Screener (OAB-V8)questionnaire. Through study completion, an average of 3 months