Evaluation of Non-Compressive Myelopathy in a Sample of Egyptian Patients
1 other identifier
observational
50
1 country
1
Brief Summary
An observational study will be conducted in the Department of Neurology at AlAzhar University Hospitals To study the etiological factors of non-compressive myelopathy in a sample of Egyptian patients
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jan 2022
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2022
CompletedFirst Submitted
Initial submission to the registry
February 17, 2022
CompletedFirst Posted
Study publicly available on registry
February 25, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
July 31, 2022
CompletedFebruary 25, 2022
February 1, 2022
6 months
February 17, 2022
February 17, 2022
Conditions
Outcome Measures
Primary Outcomes (1)
To study the etiological factors of non-compressive myelopathy in a sample of Egyptian patients
study the clinico-radiological profile of Non-compressive myelopathy
6 months
Interventions
Lumbar puncture for CSF Examination
Eligibility Criteria
Patients with acute, subacute, or chronic neurologic dysfunction consistent with myelopathy
You may qualify if:
- \- Patients with acute, subacute, or chronic neurologic dysfunction (motor and sensory deficit, sphincteric involvement, and a well-defined upper sensory segmental level) consistent with myelopathy (with or without coexisting encephalopathy, neuropathy, or radiculopathy).
You may not qualify if:
- \) Patients of myelopathy who did not undergo magnetic resonance imaging (MRI) of the spinal cord. 2) Spinal cord compression on MRI explaining patient's neurologic dysfunction. 3) History of previous trauma, acute coma and patients with definite cerebral symptoms incompatible with spinal pathology (e.g., aphasia, hemianopia, neglect, facial involvement). 4) Motor neuron disease (MND) 5)Degenerative ataxias.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Al-Hussein and Sayed Galal Hospitals
Cairo, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Mohie-eldin T Mohamed, Professor
Al-Azhar Faculty of medicine
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lecturer in Neurology
Study Record Dates
First Submitted
February 17, 2022
First Posted
February 25, 2022
Study Start
January 1, 2022
Primary Completion
June 30, 2022
Study Completion
July 31, 2022
Last Updated
February 25, 2022
Record last verified: 2022-02