- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02185287
"The Urological Dysfunctions in Young Women: Inheritance of Childhood?"
Aim of the study protocol is to evaluate in a prospective investigation of health statistics if the dysfunctions of the lower urinary tract in women aged between 18 and 40 years may be the result of past urinary pediatric dysfunction. The aim is to be able to identify the "risk conditions" which, if treated properly in early childhood, to help avoid debilitating problems that manifest themselves as adults and possibly to implement a strategy of prevention.
The choice of this age group is due to the fact that it allows for easier retrieval of data, as it is presumed that the concerned can more easily remember their history of pediatric and / or have parents still young enough to ask for such information. The problems of urinary disorders in childhood era have been the subject of increased attention by pediatricians from the end of the 70s, therefore, history taking may be more complete.
A study by Fitzgerald evaluated female subjects with mean age of 56 ± 9 years, and therefore our study aim is to investigate an age group that does not appear in the literature to supplement these findings, already reported.
Ultimate goal is the need to raise awareness of Pediatric Urologists to interact with adult Urologists in order to implement a shared strategy for the management of patients with problems of impaired bladder function in order to improve the future lower urinary tract function.
Materials and Methods: A self administered questionnaire will be used in accordance with the guidelines of the International Children's Continence Society. The questionnaire consists of two parts: the first explores the history of urological clinic patient until the age of 14,in order to evaluate any symptoms reported in a specific category of typical dysfunction of childhood; the second part refers to the present together with urological disorders of sexual function which, as emerges from the data of the literature may be of relevance urological diseases detectors. The data obtained will then be subjected to statistical calculations by which will evaluate the significance of the symptoms present in childhood in relation to their penetrance in various forms of adult diseases dysfunctional bladder and / or sexual abuse, with the prediction of the evolution of the same.
The questionnaire is anonymous in order to protect privacy. The questions that comprise it have been partly extracted from the questionnaire validated by the International Children's Society Continent and partly made by the authors of this study on the basis of the scientific evidence.
Patients will be recruited from the outpatient clinic of the Urogynecology Urology Clinic, University of Perugia, while the healthy controls will be recruited by submitting a questionnaire to the women chosen to sample a healthy population of Graduate Schools found in the framework of Urology, Pediatrics and Pediatric Surgery, University of Perugia.
The Investigators defined that the statistically significant number of healthy and pathological subjects can not be less than 200 units per reference category.
The time duration of the collection of anamnestic data depend on the ability of the authors of this research in finding the subjects to be analyzed.
There are no conflicts of interest to declare, no drugs or medical equipment will be tested .
Study Overview
Status
Conditions
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Latina, Italy, 04100
- Active, not recruiting
- Urology Unit, Sapienza University of Rome
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Perugia, Italy, 06131
- Recruiting
- Urogynecology Unit, Urology Clinic, University of Perugia
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Sub-Investigator:
- Eleonora Salvini, MD
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Contact:
- Elisabetta Costantini, Associate Professor
- Phone Number: +390755783743
- Email: elisabetta.costantini@unipg.it
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Principal Investigator:
- Elisabetta Costantini, MD, Associate Professor
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Perugia, Italy, 06131
- Recruiting
- Pediatric Surgery, University of Perugia
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Contact:
- Marco Prestipino, MD
- Email: marco.prestipino@unipg.it
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Principal Investigator:
- Antonino Appignani, Professor, MD
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Sub-Investigator:
- Marco Prestipino, MD
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Any lower urinary tract symptoms
- Female aged between 18 and 40 years
Exclusion Criteria:
- Age limit
- Lower urinary tract infection
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Lower urinary tract dysfunction, female, age: 18-40 years
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Healthy female subjects, age: 18-40 years
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
International Children Continence Society Questionnaire
Time Frame: Questionnaires scores at time 0 (screening time)
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Questionnaires scores at time 0 (screening time)
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Collaborators and Investigators
Sponsor
Collaborators
Publications and helpful links
General Publications
- Kuh D, Cardozo L, Hardy R. Urinary incontinence in middle aged women: childhood enuresis and other lifetime risk factors in a British prospective cohort. J Epidemiol Community Health. 1999 Aug;53(8):453-8. doi: 10.1136/jech.53.8.453.
- Fitzgerald MP, Thom DH, Wassel-Fyr C, Subak L, Brubaker L, Van Den Eeden SK, Brown JS; Reproductive Risks for Incontinence Study at Kaiser Research Group. Childhood urinary symptoms predict adult overactive bladder symptoms. J Urol. 2006 Mar;175(3 Pt 1):989-93. doi: 10.1016/S0022-5347(05)00416-7.
- Falconer C, Ekman-Ordeberg G, Hilliges M, Johansson O. Decreased innervation of the paraurethral epithelium in stress urinary incontinent women. Eur J Obstet Gynecol Reprod Biol. 1997 Apr;72(2):195-8. doi: 10.1016/s0301-2115(96)02685-1.
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2199/13 Prot.N.1625/13/ON
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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