Cerebrospinal Fluid Congestion in Spinal Stenosis Patients

The recruitment status of this study is unknown because the information has not been verified recently.
Verified June 2012 by Seoul National University Hospital.
Recruitment status was  Not yet recruiting
Sponsor:
Information provided by (Responsible Party):
Seoul National University Hospital
ClinicalTrials.gov Identifier:
NCT01630382
First received: June 26, 2012
Last updated: June 27, 2012
Last verified: June 2012
  Purpose

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


Condition
Spinal Stenosis

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Prospective

Resource links provided by NLM:


Further study details as provided by Seoul National University Hospital:

Primary Outcome Measures:
  • CSF pressure at spinal canal [ Time Frame: on time of recruitment ] [ Designated as safety issue: No ]
    We can calculate CSF pressure at spinal canal by using phase contraast magnetic resonance image technique.


Estimated Enrollment: 30
Study Start Date: June 2012
Estimated Study Completion Date: December 2013
Estimated Primary Completion Date: May 2013 (Final data collection date for primary outcome measure)
  Eligibility

Ages Eligible for Study:   30 Years to 70 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

study group : spinal stenosis patient control group : matched sex, age

Criteria

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
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01630382

Locations
Korea, Republic of
Seoul National University Hospital Not yet recruiting
Seoul, Korea, Republic of
Contact: Keewon Kim    +82-2-2072-2619    kdkdkd1@hanmail.net   
Sponsors and Collaborators
Seoul National University Hospital
  More Information

No publications provided

Responsible Party: Seoul National University Hospital
ClinicalTrials.gov Identifier: NCT01630382     History of Changes
Other Study ID Numbers: H-1203-088-402
Study First Received: June 26, 2012
Last Updated: June 27, 2012
Health Authority: Korea: Food and Drug Administration

Additional relevant MeSH terms:
Constriction, Pathologic
Spinal Stenosis
Bone Diseases
Musculoskeletal Diseases
Pathological Conditions, Anatomical
Spinal Diseases

ClinicalTrials.gov processed this record on October 20, 2014