Examining Bladder Control Using Magnetic Resonance Imaging (MRI) and Diffusion Tensor Imaging (DTI)
NCT ID: NCT01110278
Last Updated: 2017-08-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
47 participants
OBSERVATIONAL
2010-05-31
2012-06-22
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
CROSS_SECTIONAL
Study Groups
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Urge Incontinent Women
Women with documented urge/urgency incontinence with established care at the Oregon Health and Science University.
No interventions assigned to this group
Control Women
Women with no urge/urgency incontinence with established care at the Oregon Health and Science University.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Without a history of incontinence surgery
* Have current overactive bladder symptoms including urgency and urgency incontinence daily for the previous three months (must answer "about once a day to Question A1:how often do you leak urine, on initial screening questionnaire, and "3 or more months to question A2: How long have you experienced accidental leakage, and "yes" to question A3:Do you usually experience urinary leakage associated with feeling of urgency).
* Documented detrusor overactivity by urodynamic study within 3 months of the study is required.
* Patients who have a history of past anticholinergic therapy will be included as long as they have been off medication for 2 weeks prior to imaging.
* Female gynecology patients between age 40 and 85.
* Without a history of urinary incontinence (must answer "never" to question A1: how often do you leak urine, on initial screening questionnaire).
* Without a history of incontinence surgery.
* Without a history of overactive bladder.
* Without pelvic pain.
* Without irritative bladder symptoms (must say "no" to question A4: do you experience frequent urination on initial screening questionnaire).
Exclusion Criteria
* Past or present overt neurological disease such as history of stroke, epilepsy, MS, spinal cord injury.
* History of pelvic irradiation or bladder cancer.
* Current urinary tract infection.
* Current pelvic pain disorder.
CONTROL GROUP: This group will include 25 gynecology patients without a history of any urinary incontinence symptoms.
* Medical contraindications for MRI scanning.
* Past or present overt neurological disease such as history of stroke, epilepsy, MS, spinal cord injury.
* History of pelvic irradiation or bladder cancer.
* Current urinary tract infection.
* Current pelvic pain disorder.
40 Years
85 Years
FEMALE
Yes
Sponsors
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Pfizer
INDUSTRY
Oregon Health and Science University
OTHER
Responsible Party
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Rahel Nardos
MD
Principal Investigators
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Rahel Nardos, M.D.
Role: PRINCIPAL_INVESTIGATOR
Oregon Health and Science University
Locations
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Oregon Health & Science University
Portland, Oregon, United States
Countries
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Other Identifiers
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OHSU eIRB 6005
Identifier Type: -
Identifier Source: org_study_id
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