Spine device study pulled before it began
NCT ID NCT05944081
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study was designed to check how well the Arcadius XP L spine fusion device works and if it is safe for people with chronic low-back pain from conditions like degenerative disc disease or instability. The plan was to follow 60 patients for at least one year after surgery. However, the study was withdrawn before any patients were enrolled, so no new data was collected.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
Active substance
Arcadius XP L interbody fusion device
Disclaimer
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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.
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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Locations
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Medius Klinik Nürtingen
Nürtingen, Baden-Wurttemberg, 72622, Germany
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Rems-Murr-Klinik Schorndorf
Schorndorf, Baden-Wurttemberg, 73614, Germany
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Schelztor-Klinik Esslingen
Esslingen am Neckar, Baden-Wurttemberg, 73728, Germany