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New CT method could slash radiation in bone scans
NCT ID NCT01800084
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a newer CT reconstruction method (ASIR) can produce bone SPECT-CT images as good as the standard method (FBP) while using less radiation. Researchers enrolled 75 patients scheduled for a SPECT-CT exam. They compared image quality by measuring signal and noise in the spine and aorta. The goal was to see if ASIR could reduce radiation exposure without sacrificing image clarity.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Adaptive statistical iterative reconstruction (ASIR) and filtered back projection (FBP) reconstruction methods
- What this could lead to
- If successful, this could allow doctors to use lower radiation doses during bone SPECT-CT scans without losing image quality, making scans safer for patients.
- What could go wrong
- This is a small, completed study focused on image quality, not on patient health outcomes. The results may not apply to all types of scans or 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.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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75 people
The number who actually took part.
- Start date
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Aug 2013
- Finished
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May 2014
- Lead sponsor
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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.
- 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: * The patient must have given his/her informed and signed consent * The patient must be insured or beneficiary of a health insurance plan * A SPECT-CT exam is scheduled for the patient * The patient is able to withstand an extended position with the arms behind the head for 15 minutes (i.e. patient is able to undergo a SPECT-CT exam) Exclusion Criteria: * The patient is participating in another study * The patient is in an exclusion period determined by a previous study * The patient is under judicial protection, or any kind of guardianship * The patient refuses to sign the consent * The patient has a contra-indication for a treatment necessary for this study (patient is not able to withstand an extended position with the arms behind the head for 15 minutes) * It is impossible to correctly inform the patient * The patient is pregnant, parturient, or breastfeeding * Emergency situations * Presence of osteosynthesis material (or any other material that would generate an artifact during SPECT-CT) in the spine * Patient behaviour hampers image acquisition
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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
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CHU de Nîmes - Hôpital Universitaire Carémeau
Nîmes, Gard, 30029, France
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