Neuro-Orthopedic Registry of the University Hospital of Toulouse

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03329872

Enrollment

976

Registered

2017-11-06

Start date

2014-11-30

Completion date

2019-04-30

Last updated

2019-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neurologic Disorder

Keywords

Neuro-Orthopedics, Register

Brief 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.

Interventions

OTHERData collection

data collection about symptoms without any specific clinical or biological intervention

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Healthy volunteers

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.

Design outcomes

Primary

Measure	Time frame	Description
Neurologic symptoms	Each year until five years	Data collection

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026