Positron Emission Tomography (PET) in Evaluating Cerebral Glucose Metabolism and Functional Change for Patients With Spinal Cord Injury
PET in Evaluating Cerebral Glucose Metabolism and Functional Change for Patients With Spinal Cord Injury
2 other identifiers
observational
160
1 country
1
Brief Summary
Background: Spinal cord injury (SCI) results in dysfunction of motor and sensory system and the hormonal secretion. Not only the change of peripheral hormonal organs, the central neurotransmitters were also affected. We consider there are some changes in cerebral physiology, anatomy or function after SCI. Objective: Use PET imaging to investigate the brain functional difference among the SCI and control group.
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 Aug 2007
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
August 1, 2007
CompletedFirst Submitted
Initial submission to the registry
June 26, 2009
CompletedFirst Posted
Study publicly available on registry
June 29, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2011
CompletedDecember 1, 2010
November 1, 2010
4 years
June 26, 2009
November 30, 2010
Conditions
Keywords
Study Arms (4)
spinal cord injury 1
spinal cord injury 2
spinal cord injury 3
normal control
Eligibility Criteria
right handed patients with spinal cord injury
You may qualify if:
- age above 18 years old
- spinal cord injury for over 1 year
You may not qualify if:
- epilepsy
- psychiatric disorder
- history of central neurologic system infection
- Parkinson's disease
- Alcoholic disease
- vitamine deficiency
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Taiwan University Hospital
Taipei, Taiwan, 100, Taiwan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Yen-Ho Wang, M.D
National Taiwan University Hospital
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
June 26, 2009
First Posted
June 29, 2009
Study Start
August 1, 2007
Primary Completion
August 1, 2011
Study Completion
December 1, 2011
Last Updated
December 1, 2010
Record last verified: 2010-11