Male Stress Urinary Incontinence Clinical Trial
Official title:
Prospective Study of Urethral Mobility in Male Stress Urinary Incontinence Pre- and Post- Placement of Transobturator Sling
NCT number | NCT01779323 |
Other study ID # | Pro00026977 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | March 2012 |
Est. completion date | September 2014 |
Verified date | March 2016 |
Source | Duke University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The hypothesis is men with stress urinary incontinence, including those following radical retropubic prostatectomy and other prostate surgery, have preoperative urethral mobility as measured by magnetic resonance imaging (MRI) that improves significantly following sling placement. The investigators theorize that the sling helps with primary hypermobility of this pathophysiologic cause of stress urinary incontinence.
Status | Completed |
Enrollment | 34 |
Est. completion date | September 2014 |
Est. primary completion date | September 2014 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 45 Years and older |
Eligibility | Inclusion Criteria: - The control group: - normal male subjects - The Intervention group: - male - with stress urinary incontinence - 45 years or older - history of prior radical prostatectomy - complains of stress urinary incontinence - scheduled for a transobturator sling surgery - ability and willingness to provide written consent Exclusion Criteria: - absolute or relative contraindications to MRI - claustrophobia - inability to undergo the male sling surgery - PI judgement Absolute contraindications to MRI: - electronically, magnetically, and mechanically activated implants - ferromagnetic or electronically operated active devices - metallic splinters in the eye - ferromagnetic hemostatic clips in the central nervous system Relative contraindications to MRI: - cochlear implants - other pacemakers - nerve stimulators - lead wires or similar wires - prosthetic heart valves - hemostatic clips - non-ferromagnetic stapedial implants |
Country | Name | City | State |
---|---|---|---|
United States | Duke University Medical Center | Durham | North Carolina |
Lead Sponsor | Collaborator |
---|---|
Duke University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in urethral mobility | Measure change in urethral mobility from baseline versus 2-5 months post-surgery versus no surgical intervention. | Within 2-5 months after enrollment |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05771168 -
Surgery for Male Stress Urinary Incontinence
|
||
Completed |
NCT02288455 -
Clinical Investigation of GT UrologIcal, LLC's Artificial Urinary Sphincter (RELIEF II)
|
N/A |