Cystocele Clinical Trial
— LUTS-2Official title:
Lower Urinary Tract Symptoms Screening Questionnaire Validation STudy
NCT number | NCT01616810 |
Other study ID # | 04-227 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | January 2007 |
Est. completion date | December 2011 |
Verified date | February 2019 |
Source | St. Michael's Hospital, Toronto |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The purpose of this study is to determine the validity of a screening tool which has been designed to detect the presence or absence of lower urinary tract symptoms in the general female population.
Status | Completed |
Enrollment | 300 |
Est. completion date | December 2011 |
Est. primary completion date | October 2007 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Healthy participants, 18 years of age and older with any gynecological symptoms Exclusion Criteria: - Patients with lower urinary tract symptoms and pelvic floor dysfunction |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
St. Michael's Hospital, Toronto |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Presence or absence of lower urinary tract symptoms in the general female population | To validate the effectiveness of a screening tool in detecting the presence or absence of lower urinary tract symptoms in the general female population. | Five years |
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