We updated the design of this site on September 25th. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

Cerebrospinal Fluid Congestion in Spinal Stenosis Patients

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified June 2012 by Seoul National University Hospital.
Recruitment status was:  Not yet recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT01630382
First Posted: June 28, 2012
Last Update Posted: June 28, 2012
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Seoul National University Hospital
  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 ]
    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

Information from the National Library of Medicine

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, Learn About Clinical Studies.


Ages Eligible for Study:   30 Years to 70 Years   (Adult, Senior)
Sexes Eligible for Study:   All
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
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): 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

Responsible Party: Seoul National University Hospital
ClinicalTrials.gov Identifier: NCT01630382     History of Changes
Other Study ID Numbers: H-1203-088-402
First Submitted: June 26, 2012
First Posted: June 28, 2012
Last Update Posted: June 28, 2012
Last Verified: June 2012

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