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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 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.

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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.

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

FieldValue
Enrollment Target 100 participants
Start Date 2025-03-04
Est. Completion 2025-05-30

Sponsor

Silony Medical

2 total trials

What the Registry Record Tells You About NCT06876311

The ClinicalTrials.gov registry entry for NCT06876311 describes a study currently listed as active not recruiting, categorized as an unspecified phase. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Silony Medical, which has 2 total studies on file at ClinicalTrials.gov.

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 1 study location spanning 1 distinct geographic area - top geographies include 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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.