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NCT01324622 · ClinicalTrials.gov registry record · NA
Comparison of Cervical Laminectomy to Laminoplasty
A NA study, sponsored by Synthes USA HQ.
- Terminated
- Registry status
- NA
- Development phase
- 24
- Enrollment target
NCT01324622 is a NA study that was terminated before completion, run by Synthes USA HQ. The registered enrollment target is 24 participants.
The verdict
NCT01324622, a NA study, was terminated before completion, sponsored by Synthes USA HQ.
- TERMINATED
- Registry status
- NA
- Development phase
- 24 participants
- Enrollment target
Study Summary
The objective of this study is to compare the clinical and radiographic outcomes of multi-level laminectomy to multi-level laminoplasty in the treatment of patients with cervical myelopathy or myeloradiculopathy. The hypothesis for the study is that the laminoplasty group is not inferior to the laminectomy group.
Interventions
- DEVICE Laminoplasty
- PROCEDURE laminectomy
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 24 participants |
| Start Date | 2006-01-01 |
| Est. Completion | 2010-11-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01324622
The ClinicalTrials.gov registry entry for NCT01324622 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 24 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Synthes USA HQ, which has 7 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Laminoplasty is the first listed.
NCT01324622 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01324622 about?
NCT01324622 is a clinical study titled "Comparison of Cervical Laminectomy to Laminoplasty". The objective of this study is to compare the clinical and radiographic outcomes of multi-level laminectomy to multi-level laminoplasty in the treatment of patients with cervical myelopathy or myeloradiculopathy. The hypothesis for the study is that the laminoplasty group is not inferior to the lami...
What is the current status of trial NCT01324622?
This trial is currently terminated. It is a NA study. The enrollment target is 24 participants. The study started on 2006-01-01. Estimated completion is 2010-11-01.
What interventions are being tested in trial NCT01324622?
The interventions under investigation include: Laminoplasty (DEVICE), laminectomy (PROCEDURE).
Who is sponsoring clinical trial NCT01324622?
This trial is sponsored by Synthes USA HQ, which has 7 total clinical trials registered on ClinicalTrials.gov.
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