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Clinical Trial Details — Status: Completed

Administrative data

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

Study information

Verified date March 2016
Source Duke University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

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

Study Design


Intervention

Other:
Pre and Post Sling Pelvic MRI
Pre and Post Sling Pelvic MRI

Locations

Country Name City State
United States Duke University Medical Center Durham North Carolina

Sponsors (1)

Lead Sponsor Collaborator
Duke University

Country where clinical trial is conducted

United States, 

Outcome

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
See also
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