Neuro-Orthopedic Registry of the University Hospital of Toulouse
NCT ID: NCT03329872
Last Updated: 2019-07-16
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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COMPLETED
976 participants
OBSERVATIONAL
2014-11-30
2019-04-30
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
Study Groups
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Patients group
Patients follow-up in hospital will have data collection
Data collection
data collection about symptoms without any specific clinical or biological intervention
Interventions
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Data collection
data collection about symptoms without any specific clinical or biological intervention
Eligibility Criteria
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Inclusion Criteria
* An injection of botulinum toxin in the context of spasticity : about 20 / week
* Pre or post-therapeutic clinical evaluation (botulinum toxin or surgery): approximately 10 / week
* Clinical or instrumental evaluation of the walking or upper limb (Physiological Functional Explorations): about 10 / week
* A medical and surgical multidisciplinary consultation about spasticity : about 15 / month
* A discussion during neuroorthopedic multidisciplinary consultation meeting about the patient's file and anomalies of walking: about 8 / month
* Implementation of a Baclofen pump (Neurosurgery): about 2 / month
* Functional surgery of the upper or lower limb (locomotor institute, orthopedic surgery and traumatology): about 4 / sem
Exclusion Criteria
ALL
No
Sponsors
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Ipsen
INDUSTRY
University Hospital, Toulouse
OTHER
Responsible Party
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Principal Investigators
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David Gasq
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Toulouse
Locations
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CHU de Toulouse
Toulouse, Midi-Pyrénées, France
Countries
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Other Identifiers
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14 7321 03
Identifier Type: -
Identifier Source: org_study_id
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