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NCT06876311 · ClinicalTrials.gov registry record
Observational Study to Evaluate the STALIF® C FLX, STALIF® M FLX, STALIF® L FLX Cages and FORTOS-C®
A clinical trial of Degenerative Cervical Disc Disease and Degenerative Lumbar Diseases, sponsored by Silony Medical.
- Active
- Registry status
- 100
- Enrollment target
- 1
- Study location
NCT06876311: Active study of Degenerative Cervical Disc Disease and Degenerative Lumbar Diseases, sponsored by Silony Medical.
NCT06876311 is a study of Degenerative Cervical Disc Disease and Degenerative Lumbar Diseases that is active but no longer recruiting, run by Silony Medical. The registered enrollment target is 100 participants. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06876311, a study of Degenerative Cervical Disc Disease and Degenerative Lumbar Diseases, is active but no longer recruiting, sponsored by Silony Medical.
- ACTIVE NOT RECRUITING
- Registry status
- 100 participants
- Enrollment target
- 1
- Study location
Study Summary
Post-operative clinical outcome data on the devices used to treat spinal diseases are collected and evaluated in order to analyze the safety and performance of the implants used.
Primary Outcome
The Neck Disability Index (NDI) has 10 items that cover various aspects of daily functioning, such as pain, personal care, lifting, reading, headaches, concentration, work, driving, sleeping and recreation. Scoring: Each question contains six answer choices, scored from 0 (no disability) to 5 (complete disability). All section scores are then totaled. Scoring is reported on a 0-50 scale, 0 being the best possible score and 50 being the worst. Alternately, the score can be reported from 0-100. T
Conditions Studied
Interventions
- DEVICE Anterior Cervical Interbody Fusion
- DEVICE Anterior lumbar Interbody Fusion
- DEVICE Lateral Lumbar Interbody Fusion
Study Locations (1)
California
- Golden State Orthopedics and Spine - San Ramon
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2025-03-04 |
| Est. Completion | 2025-05-30 |
What the registry record for NCT06876311 still lists
NCT06876311 is an observational study that tracks outcomes without assigning an intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap.
The record links to 2 conditions, with Degenerative Cervical Disc Disease appearing as the primary indexed condition, and to 3 interventions - of which Anterior Cervical Interbody Fusion is the first listed.
NCT06876311 reports a single indexed study location in California.
Frequently Asked Questions
What is clinical trial NCT06876311 about?
NCT06876311 is a clinical study titled "Observational Study to Evaluate the STALIF® C FLX, STALIF® M FLX, STALIF® L FLX Cages and FORTOS-C®". Post-operative clinical outcome data on the devices used to treat spinal diseases are collected and evaluated in order to analyze the safety and performance of the implants used.
What is the current status of trial NCT06876311?
This trial is currently active not recruiting. The enrollment target is 100 participants. The study started on 2025-03-04. Estimated completion is 2025-05-30.
What conditions does trial NCT06876311 study?
This clinical trial studies the following conditions: Degenerative Cervical Disc Disease, Degenerative Lumbar Diseases.
What interventions are being tested in trial NCT06876311?
The interventions under investigation include: Anterior Cervical Interbody Fusion (DEVICE), Anterior lumbar Interbody Fusion (DEVICE), Lateral Lumbar Interbody Fusion (DEVICE).
Who is sponsoring clinical trial NCT06876311?
This trial is sponsored by Silony Medical, which has 2 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06876311 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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