New study aims to take the guesswork out of spinal fusion healing
NCT ID NCT05565456
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows 30 adults aged 45-80 who are having spinal fusion surgery for spondylolisthesis. Researchers will use CT scans to measure changes in the bone graft placed between vertebrae over time. The goal is to develop an objective way to assess whether the bones have fused properly, which is currently difficult to determine.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- autologous bone graft
- What this could lead to
- If successful, this could lead to a reliable, objective way to measure bone healing after spinal fusion surgery, helping doctors assess fusion status without guesswork.
- What could go wrong
- This is a small, observational study with only 30 participants. It does not test a new treatment, so it may not directly change patient care. The results may not apply to all spinal fusion patients.
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
-
30 people
The number who actually took part.
- Started
-
Dec 2022
- Expected to finish
-
Nov 2026
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Thirty patients with a symptomatic spondylolisthesis (lytic/degenerative/iatrogenic) who have an indication for single level lumbar interbody fusion (PLIF/TLIF) will be recruited.
- Ages
-
45 to 80 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria: * non-responsiveness to non-operative treatment in the six months prior to study enrolment * fusion indicated for only one segment in the L1 to S1/ilium region * between the age of 45 and 80. Exclusion criteria: * receiving revision spine surgery * not wanting to provide informed consent * pregnant or expecting to be pregnant within in the next two years.
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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
Locations
-
Rijnstate Hospital
Arnhem, Gelderland, 6800 WC, Netherlands
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a brace and targeted exercises ease spondylolisthesis pain?
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