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NCT01630382 Clinical Trial

Cerebrospinal Fluid Congestion in Spinal Stenosis Patients

Spinal Stenosis Clinical Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT01630382
Other study ID # H-1203-088-402
Secondary ID
Status Not yet recruiting
Phase N/A
First received June 26, 2012
Last updated June 27, 2012
Start date June 2012
Est. completion date December 2013

Study information
Verified date June 2012
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority Korea: Food and Drug Administration
Study type Observational

Clinical Trial Summary

The investigators hypothesized spinal stenosis symptom was provocation due to cerebrospinal fluid congestion.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 30
Est. completion date December 2013
Est. primary completion date May 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 30 Years to 70 Years
Eligibility Inclusion Criteria:

- neurogenic claudication more than 3months

- relief neurogenic claudication by lumbar flexion

- spinal stenosis symptom by physical exam.

- who can walk more than 30 min.

Exclusion Criteria:

- vascular claudication by physical exam.( ABI <0.9)

- structural change in vertebral ( tumor, congenital deformity)

- operation history at spinal bone

- metallic foreign body

- peripheral polyneuropathy

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (1)
Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary CSF pressure at spinal canal We can calculate CSF pressure at spinal canal by using phase contraast magnetic resonance image technique. on time of recruitment No
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