Stimulating Catheter With or Without Ultrasound Guidance
NCT ID: NCT00980577
Last Updated: 2010-11-10
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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UNKNOWN
PHASE4
100 participants
INTERVENTIONAL
2008-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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NS
stimulating catheter will be inserted using stimulator
NUUS
Sonosite Micro Maxx
Interventions
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NUUS
Sonosite Micro Maxx
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Able to give informed consent
* Able to cooperate with sensory and motor testing of lower limb function
Exclusion Criteria
* Allergy to local anaesthetic or postanalgesic rescue regimen
* Signs, symptoms or laboratory evidence of local infection or systemic sepsis
* No pre-existing neurological deficit (sensory or motor) affecting lower limb
* Patients with lower limb amputations
30 Years
90 Years
ALL
No
Sponsors
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Peking University Third Hospital
OTHER
Responsible Party
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Peking University Health Science Center Review Board
Locations
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Peking University Third Hosptial
Beijing, , China
Countries
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Central Contacts
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Other Identifiers
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PUTH7275
Identifier Type: -
Identifier Source: org_study_id