NCT00629655

Brief Summary

The spinal cord is a very important part of the central nervous system. fMRI can be applied to observe functional status of the human spinal cord. Under different conditions, the investigators will see different types of fMRI signals within the spinal cord. In resting state, the investigators might see active/inactive signals, too.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
22

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Feb 2008

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2008

Completed
26 days until next milestone

First Submitted

Initial submission to the registry

February 27, 2008

Completed
8 days until next milestone

First Posted

Study publicly available on registry

March 6, 2008

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2009

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2009

Completed
Last Updated

June 5, 2009

Status Verified

June 1, 2009

Enrollment Period

1.2 years

First QC Date

February 27, 2008

Last Update Submit

June 4, 2009

Conditions

Cerebral Infarction

Keywords

fMRIspinal cordhumanhealthcerebral infarctionhealthy

Outcome Measures

Primary Outcomes (1)

  • fMRI

    one day

Study Arms (2)

1

healthy people, male

Other: motor task, sensory stimulation

2

male patients with cerebral infarction, chronic stage

Other: motor task, sensory stimulation

Interventions

motor task, sensory stimulationOTHER

motor task: finger tapping, simple type and complex type sensory stimulation: electric or tactile stimulation

Also known as: group 1:healthy people, group 2:patients with cerebral infarction,chronic stage
12

Eligibility Criteria

Age18 Years - 45 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

group 1: male residents of Beijing group 2: male stroke patients of Beijing Boai hospital

You may qualify if:

  • Chinese male residents
  • right handed
  • no history of psychological/psychotic problems
  • no history of important diseases

You may not qualify if:

  • with factors which make subjects unsuitable to receive MR examination
  • history of important diseases
  • Chinese male patients with ischemic stroke (CT/MRI scan confirmed)
  • right handed
  • at least 1.5 months from onset of stroke
  • ability to follow complex commands
  • hemodynamic instability
  • history of dementia
  • inability to give consent because of impaired cognition or receptive aphasia
  • diseases in spine/spinal cord
  • with factors which make subjects unsuitable to receive MR examination

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Beijing Boai Hospital

Beijing, Beijing Municipality, 100068, China

Location

MeSH Terms

Conditions

Cerebral Infarction

Condition Hierarchy (Ancestors)

Brain InfarctionBrain IschemiaCerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesStrokeVascular DiseasesCardiovascular DiseasesInfarctionIschemiaPathologic ProcessesPathological Conditions, Signs and SymptomsNecrosis

Study Officials

  • Pengxu Wei, Master

    China Rehabilitation Research Center

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER GOV

Study Record Dates

First Submitted

February 27, 2008

First Posted

March 6, 2008

Study Start

February 1, 2008

Primary Completion

April 1, 2009

Study Completion

April 1, 2009

Last Updated

June 5, 2009

Record last verified: 2009-06

Locations

CN(1)