New neck implant under study: will it ease pain and improve lives?
NCT ID NCT05296889
First seen Jun 27, 2026 · Last updated Aug 04, 2026 · Updated 2 times
Summary
This study is tracking 200 adults who receive the Ennovate Cervical Spinal System, a metal implant used to stabilize the neck and upper back after fractures, disc disease, or tumors. Researchers will measure changes in pain and quality of life over time. The goal is to confirm the device works safely in everyday medical practice.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Ennovate® Cervical Spinal System (a metal implant device for stabilizing the neck and upper back spine)
- What this could lead to
- If successful, this study could confirm that the Ennovate Cervical system is a safe and effective option for stabilizing the spine and reducing pain in people with various neck spine conditions.
- What could go wrong
- This is an observational post-market study, not a randomized trial, so it cannot prove the device is better than other treatments. Results depend on patient reports and may not apply to everyone.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2021
- Expected to finish
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Sep 2028
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
All patients treated with the Ennovate® Cervical system in accordance with the indications given in the instructions for use: fractures, degenerative instability, post-trauma instability, tumors, degenerative cervical myelopathy
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient is minimum 18 years old * Informed Consent in the documentation of clinical and radiological results * Patient has indication according to Instructions for Use (IFU) * Patient is not pregnant Exclusion Criteria: * Patient's clear unability or unwillingness to participate in follow-up examinations
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
3 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Berufsgenossenschaft Klinikum Bergmannstrost Halle / Saale
RECRUITINGHalle, Saxony-Anhalt, 06112, Germany
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Krankenhaus Ludmillenstift Meppen
NOT_YET_RECRUITINGMeppen, Lower Saxony, 49716, Germany
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Schön Klinik Hamburg Eilbek
ACTIVE_NOT_RECRUITINGHamburg, Free and Hanseatic City of Hamburg, 22081, Germany
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Städtisches Klinikum Dresden
NOT_YET_RECRUITINGDresden, Saxony, 01076, Germany
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