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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT00441935 |
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Date of registration:
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28/02/2007 |
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Primary sponsor: |
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Public title:
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InterStim Prospective Database
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Scientific title:
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InterStim Prospective Database for Outcomes Research |
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Date of first enrolment:
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April 2004 |
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Target sample size:
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3000 |
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Recruitment status: |
Enrolling by invitation |
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URL:
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http://clinicaltrials.gov/show/NCT00441935 |
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Study type:
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Observational |
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Study design:
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Time Perspective: Prospective
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Countries of recruitment
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United States
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Contacts
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Name:
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Kenneth Peters, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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William Beaumont Hospitals |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- All patients at least 18 years of age scheduled for sacral nerve stimulator
implantation at William Beaumont Hospital, Royal Oak, Michigan who give informed
consent to participate in the project.
Exclusion Criteria:
- None
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Pelvic Pain
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Urinary Incontinence
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Urinary Retention
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Intervention(s)
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Device: InterStim Neuromodulation
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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