Neurologic and Neurophysiologic Assessment of Clinical Course in Patients With Intraspinal Processes
1 other identifier
observational
100
1 country
1
Brief Summary
Patients included in the study are treated at the Klinik für Neurochirurgie USZ. The clinical course is documented at Paraplegikerzentrum Balgrist using validated diagnostic procedures (e.g. SCIM, ASIA, neurophysiology). Study aims: Prognostic value of clinical diagnosis and additional diagnostic procedures? Which parameters exhibit optimal prognostic power? Differences between tumor/AVM associated lesions and traumatic lesions? What can we learn for pathophysiology and treatment?
- Trial with surgical intervention
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jan 2010
Longer than P75 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, 2010
CompletedFirst Submitted
Initial submission to the registry
April 15, 2010
CompletedFirst Posted
Study publicly available on registry
April 16, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2015
CompletedApril 16, 2010
April 1, 2010
April 15, 2010
April 15, 2010
Conditions
Keywords
Study Arms (1)
intralspinal processes
Patients with intralspinal processes
Interventions
SCIM Spinal Cord Independence Measure ASIA scale American Spinal Injury Association
Eligibility Criteria
Patients treated surgically for intraspinal processes
You may qualify if:
- Benign intraspinal process (tumor or vascular malformation AVM)
- Primary lesion caudal of the brainstem, affecting C1
- Cognitive ability to give written informed consent
You may not qualify if:
- Metastases, malign tumors
- Traumatic lesions
- Myelitis, polyneuropathy
- Disc prolaps
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Unknown Facility
Zurich, Switzerland
MeSH Terms
Conditions
Study Officials
- STUDY DIRECTOR
01 Studienregister MasterAdmins
UniversitaetsSpital Zuerich
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
April 15, 2010
First Posted
April 16, 2010
Study Start
January 1, 2010
Study Completion
December 1, 2015
Last Updated
April 16, 2010
Record last verified: 2010-04