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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01293110
Other study ID # KEK-2010-0207/0/PB_2016-0189
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 2010
Est. completion date January 2030

Study information

Verified date May 2024
Source University of Zurich
Contact Thomas M Kessler, MD
Phone +41 44 386 39 07
Email thomas.kessler@balgrist.ch
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Patients with neurological disease/injury often suffer from lower urinary tract symptoms, which frequently have a negative impact on the patients' health related quality of life. The prevalence of lower urinary tract dysfunction is high and the treatment is a challenge because available treatments may fail. In this study data of patients with lower urinary tract dysfunction treated at the University of Zürich, are prospectively and systematically collected in a database.


Description:

Lower urinary tract dysfunction is characterized by detrusor overactivity, detrusor sphincter dyssynergia, voiding dysfunction, stress incontinence, or a combination of these and frequently has a negative impact on the patients' health related quality of life. In addition, the treatment of lower urinary tract dysfunction is a challenge because conventional therapies may fail. Adequate treatment and long-term follow-up of lower urinary tract dysfunction is important to achieve/maintain continence and preserve renal function. Thus, we aim to prospectively collect clinical, video-urodynamic and radiological data of patients with neurogenic lower urinary tract dysfunction treated at the University of Zürich in a database.


Recruitment information / eligibility

Status Recruiting
Enrollment 7000
Est. completion date January 2030
Est. primary completion date January 2030
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - patient of Balgrist University Hospital - patient of University Hospital Zürich - urodynamic examination - written informed consent Exclusion Criteria: - no written informed consent

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Switzerland Spinal Cord Injury Center & Research, University of Zürich, Balgrist University Hospital Zürich

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Survival of the patients first visit to death
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