Assessment of Surgical Techniques for Treating Cervical Spondylotic Myelopathy
Public ClinicalTrials.gov record NCT00285337. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
An Assessment of Surgical Techniques for Treating Cervical Spondylotic Myelopathy
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
The primary purpose of this study is to compare anterior and posterior surgical approach in treatment of CSM in terms of surgical complications and neurological, functional, disease-specific and quality of life outcomes measures. Secondary aims are to quantify the amount of change pre and post-surgery concerning the same outcome measures; to determine if there are differences in outcomes between posterior surgical techniques (i.e. laminectomy with fusion or laminoplasty) and examine the relationship between baseline MRI and baseline and follow-up neurological and functional outcomes.
Study identification
- NCT ID
- NCT00285337
- Recruitment status
- Completed
- Study type
- Observational
- Phase
- Not listed
- Enrollment
- 321 participants
Conditions and interventions
Conditions
Eligibility (public fields only)
- Age range
- Not listed
- Sex
- All
- Healthy volunteers
- Accepts healthy volunteers
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Dec 2005 (Type not available)
- Primary completion
- Not listed
- Completion
- Nov 2007 (Actual)
- Last update posted
- Nov 1, 2017
2005 – 2007
United States locations
- U.S. sites
- 12
- U.S. states
- 11
- U.S. cities
- 11
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Spine Education and Research Institute | Thornton | Colorado | 80229 | — |
| Emory University | Atlanta | Georgia | 30329 | — |
| Indianda Spine Group | Indianapolis | Indiana | 46260 | — |
| Kansas University Medical Center | Kansas City | Kansas | 66160 | — |
| John Hopkins University | Baltimore | Maryland | 21287 | — |
| Brigham and Women's Hospital | Boston | Massachusetts | 02115 | — |
| New England Baptist Hospital | Boston | Massachusetts | 02120 | — |
| Mayo Clinic | Rochester | Minnesota | 55905 | — |
| Thomas Jefferson University and Rothman Institure Orthopaedics | Philadelphia | Pennsylvania | 19107 | — |
| Universty of Utah | Salt Lake City | Utah | 84108 | — |
| University Of Virginia | Charlottesville | Virginia | 22908 | — |
| Harborview Medical Center | Seattle | Washington | 98104 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
Non-U.S. locations
This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT00285337, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Nov 1, 2017 · Synced Oct 23, 2026
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Open the official record
The complete public registry record, listed eligibility criteria, and available contact information for NCT00285337 live on ClinicalTrials.gov.