Neuro-Orthopedic Registry of the University Hospital of Toulouse

Neurologic Disorder Clinical Trial

Official title:

Neuro-Orthopedic Registry of the University Hospital of Toulouse

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03329872
• Other study ID #: 14 7321 03
• Status: Completed
• Start date: November 2014
• Est. completion date: April 2019

Study information

• Verified date: July 2019
• Source: University Hospital, Toulouse
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

Neuro-orthopedics corresponds to the evaluation and therapeutic management of the orthopedic consequences of damage to the central or peripheral nervous system. In case of neurological impairment, there may be joint, motor, sensory and cognitive impairments that limit the patient's activities. The management of these orthopedic problems falls within the specific framework of neuro-orthopedics because in the presence of neurological, problems are different and more complex than in classical orthopedics. In this context, a well-conducted evaluation is a prerequisite for appropriate treatment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 976
• Est. completion date: April 2019
• Est. primary completion date: April 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

Patient with a neurological condition that benefits:

• 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:

Patient (or the legal representative) who opposes the data collection.

Related Conditions & MeSH terms

• Nervous System Diseases
• Neurologic Disorder

Intervention

Other:
• Data collection
data collection about symptoms without any specific clinical or biological intervention

Locations

Country	Name	City	State
France	CHU de Toulouse	Toulouse	Midi-Pyrénées

Sponsors (2)

Lead Sponsor	Collaborator
University Hospital, Toulouse	Ipsen

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Neurologic symptoms	Data collection	Each year until five years