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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WITHDRAWN
OBSERVATIONAL
2003-04-30
2004-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* patients with spinal lesion
* patients with cauda equina syndrome
Exclusion Criteria
* pacemaker or other metallic material implanted
* epileptic patients
* organic colorectal disease
* obese patients
* previous neurological surgery
18 Years
ALL
Yes
Sponsors
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University Hospital, Rouen
OTHER
Responsible Party
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Principal Investigators
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Anne-Marie LEROI, PHD
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Rouen
Locations
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University hospital of Rouen
Rouen, , France
Countries
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Other Identifiers
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2001/099/HP
Identifier Type: -
Identifier Source: org_study_id
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