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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