Bone device study ends early, but data still collected
NCT ID NCT07087509
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at a medical device called TriOSS® used to help heal bone defects. Researchers reviewed medical records of 23 adults who had the device implanted after trauma, surgery, or spine problems. The goal was to see how well the device helped bone heal and whether it caused any side effects. The study was stopped early, but the data will still be used to understand the device's safety and performance.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- TriOSS® (a medical device for bone regeneration)
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
-
23 people
The number who actually took part.
- Started
-
Sep 2025
- Finished
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Jan 2026
- Lead sponsor
-
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
The study population consists of adult patients (\> 18 years old) undergoing orthopaedic surgery after bone defect.
- Ages
-
18 years and older
- Sex
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Anyone
- Healthy volunteers
-
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: * Adult males or females (age \> 18 years old); * Patients with osseous defects, either of trauma origin, surgically created, or associated with spinal degenerative diseases that require segmental fusion of the spine. * Patients with bone skeletal defects that are not intrinsic to the stability of the bone structure. Exclusion Criteria: * Signs of local or systemic acute/ active or chronic infections; * Metabolic affections; * Severe degenerative diseases, conditions in which general bone grafting is not advisable; * Implementation sites that allow product migration; * Conditions which require structural support in the skeletal system; * Conditions where the implantation site is unstable and not rigidly fixated; * Sensibility to the implantable materials; * Known hypersensitivity to the implant material.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Hospital Lusíadas Lisboa
Lisbon, Portugal
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