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NCT03077516 · ClinicalTrials.gov registry record

Post-Market, Long-Term Follow Up of Mobi-C® Cervical Disc for One and Two Level Treatment of Cervical Disc Disease

A clinical trial of Cervical Disc Disease and Cervical Disc Degeneration, sponsored by LDR Spine U.

Completed
Registry status
216
Enrollment target
8
Study locations

NCT03077516: Completed study of Cervical Disc Disease and Cervical Disc Degeneration, sponsored by LDR Spine U.

NCT03077516 is a study of Cervical Disc Disease and Cervical Disc Degeneration that has completed, run by LDR Spine U. The registered enrollment target is 216 participants, above the 150-participant average among 3 other Cervical Disc Disease trials with a reported enrollment target (44% higher). The trial reports 8 study locations across 4 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03077516, a study of Cervical Disc Disease and Cervical Disc Degeneration, has completed, sponsored by LDR Spine U.

COMPLETED
Registry status
216 participants
Enrollment target
8
Study locations

Study Summary

The purpose of this study is to evaluate clinical and patient-reported outcomes at 10 years following surgery for a cohort of Mobi-C subjects treated on the IDE/Post Approval studies

Interventions

  • DEVICE Mobi-C

Study Locations (8)

California

  • Orange County Neurosurgical Associates - Laguna Hills
  • Desert Orthopedic Center - Rancho Mirage
  • UC Davis Spine Center - Sacramento
  • The Spine Institute - Santa Monica

Texas

  • Texas Back Institute - Plano
  • Texas Spine and Joint Hospital - Tyler

Indiana

  • Orthopedics Northeast - Fort Wayne

Louisiana

  • Spine Institute of Louisiana - Shreveport

Trial Details

FieldValue
Enrollment Target 216 participants
Start Date 2016-11
Est. Completion 2019-10-31
LDR Spine U

1 total trials

What the finished NCT03077516 record still lists

NCT03077516 is an observational study that tracks outcomes without assigning an intervention. The registered 216 participants enrollment target is mid-sized for trials with a published cap, above the 150-participant average among 3 other Cervical Disc Disease trials with a reported enrollment target (44% higher).

The record links to 2 conditions, with Cervical Disc Disease appearing as the primary indexed condition, and to 1 intervention - of which Mobi-C is the first listed.

NCT03077516 lists 8 locations in 4 states (California, Texas, Indiana).

Frequently Asked Questions

What is clinical trial NCT03077516 about?

NCT03077516 is a clinical study titled "Post-Market, Long-Term Follow Up of Mobi-C® Cervical Disc for One and Two Level Treatment of Cervical Disc Disease". The purpose of this study is to evaluate clinical and patient-reported outcomes at 10 years following surgery for a cohort of Mobi-C subjects treated on the IDE/Post Approval studies

What is the current status of trial NCT03077516?

This trial is currently completed. The enrollment target is 216 participants. The study started on 2016-11. Estimated completion is 2019-10-31.

What conditions does trial NCT03077516 study?

This clinical trial studies the following conditions: Cervical Disc Disease, Cervical Disc Degeneration.

What interventions are being tested in trial NCT03077516?

The interventions under investigation include: Mobi-C (DEVICE).

Who is sponsoring clinical trial NCT03077516?

This trial is sponsored by LDR Spine U, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03077516 being conducted?

This trial has 8 study locations across California, Indiana, Louisiana, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT03077516, the US trial registry maintained by the National Library of Medicine. NCT03077516 (mid enrollment · multi site footprint · completed) retrieved and formatted by PlainTrial, see methodology.