CSS-Assessing the Course of Degenerative Cervical Spinal Stenosis Using Functional Outcomes
Last updated on July 2021Recruitment
- Recruitment Status
- Enrolling by invitation
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Cervical Myelopathy
- Cervical Spinal Stenosis
- Type
- Observational
- Design
- Observational Model: CohortTime Perspective: Other
Participation Requirements
- Age
- Between 18 years and 125 years
- Gender
- Both males and females
Description
Study A is a single centre cross-sectional study with two study groups, one that will be treated conservatively (stenosis) and one that will be treated surgically (stenosis and myelopathy). Study B is a single centre longitudinal study where the same patient groups will be followed up during the cou...
Study A is a single centre cross-sectional study with two study groups, one that will be treated conservatively (stenosis) and one that will be treated surgically (stenosis and myelopathy). Study B is a single centre longitudinal study where the same patient groups will be followed up during the course of their treatment. Clinical, radiological, biomechanical (kinematic and electromyographic), neurological and neurophysiological data will be collected. Differences in and the relationship between the clinical, radiological, biomechanical, neurological and neurophysiological data will be determined .
Tracking Information
- NCT #
- NCT04381663
- Collaborators
- Not Provided
- Investigators
- Principal Investigator: Annegret Mündermann, Prof. Dr. University Hospital, Basel, Switzerland Principal Investigator: Cordula Netzer, Dr. med. University Hospital, Basel, Switzerland Principal Investigator: Regina Schläger, PD Dr. med. University Hospital, Basel, Switzerland Principal Investigator: Martin Hardmeier, PD Dr. med. University Hospital, Basel, Switzerland
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