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NCT06485206 · ClinicalTrials.gov registry record · NA

Evaluation of Safety and Effectiveness of Primary Hybrid Construct of Mobi-C and ACDF in the Treatment of Two-level Symptomatic Degenerative Disc Disease in the Cervical Spine.

A NA study of Degenerative Disc Disease, sponsored by Highridge Medical.

Recruiting
Registry status
NA
Development phase
97
Enrollment target
2
Study locations

NCT06485206 is a NA study of Degenerative Disc Disease that is actively recruiting participants, run by Highridge Medical. The registered enrollment target is 97 participants, below the 166-participant average among 42 other Degenerative Disc Disease trials with a reported enrollment target (42% lower). The trial reports 2 study locations across 2 states.

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The verdict

NCT06485206, a NA study of Degenerative Disc Disease, is actively recruiting participants, sponsored by Highridge Medical.

RECRUITING
Registry status
NA
Development phase
97 participants
Enrollment target
2
Study locations

Study Summary

The study is a prospective, multi-center cohort study of patients with two-level DDD implanted with CDA adjacent to ACDF (hybrid construct). The overall success of the hybrid procedure will be compared to 2-level ACDF historical controls from the Mobi-C IDE trial. 97 patients will receive the hybrid surgery and will be followed for a minimum of 2 years.

Conditions Studied

Interventions

  • DEVICE One level Mobi-C and one level fusion

Study Locations (2)

California

  • University of California-Davis - Sacramento

Michigan

  • Michigan Orthopaedic Surgeons - Southfield

Trial Details

FieldValue
Enrollment Target 97 participants
Start Date 2024-09-01
Est. Completion 2029-05
Phase NA

Sponsor

Highridge Medical

1 total trials

What the Registry Record Tells You About NCT06485206

The ClinicalTrials.gov registry entry for NCT06485206 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 97 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 166-participant average among 42 other Degenerative Disc Disease trials with a reported enrollment target (42% lower). The listed sponsor is Highridge Medical, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Degenerative Disc Disease appearing as the primary indexed condition, and to 1 intervention - of which One level Mobi-C and one level fusion is the first listed.

NCT06485206 reports 2 study locations spanning 2 distinct geographic areas - top geographies include California, Michigan.

Frequently Asked Questions

What is clinical trial NCT06485206 about?

NCT06485206 is a clinical study titled "Evaluation of Safety and Effectiveness of Primary Hybrid Construct of Mobi-C and ACDF in the Treatment of Two-level Symptomatic Degenerative Disc Disease in the Cervical Spine.". The study is a prospective, multi-center cohort study of patients with two-level DDD implanted with CDA adjacent to ACDF (hybrid construct). The overall success of the hybrid procedure will be compared to 2-level ACDF historical controls from the Mobi-C IDE trial. 97 patients will receive the hybrid...

What is the current status of trial NCT06485206?

This trial is currently recruiting. It is a NA study. The enrollment target is 97 participants. The study started on 2024-09-01. Estimated completion is 2029-05.

What conditions does trial NCT06485206 study?

This clinical trial studies the following conditions: Degenerative Disc Disease.

What interventions are being tested in trial NCT06485206?

The interventions under investigation include: One level Mobi-C and one level fusion (DEVICE).

Who is sponsoring clinical trial NCT06485206?

This trial is sponsored by Highridge Medical, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06485206 being conducted?

This trial has 2 study locations across California, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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