Spine device registry launches to monitor Real-World safety
NCT ID NCT05170815
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study is collecting information from 760 adults who receive ERISMA or Idys spine implants during surgery. Researchers will track complications, pain levels, and quality of life for two years after the procedure. The goal is to confirm the devices are safe and work well in everyday medical practice.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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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.
Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Santy Orthopedic Center
RECRUITINGLyon, France
Contact