Tiny power plants in cells may weaken bones, new study hints
NCT ID NCT05483738
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looks at how problems with mitochondria—the tiny power plants inside cells—might affect bone health. Researchers will compare 30 people with certain genetic changes that cause mitochondrial dysfunction to healthy volunteers. They will take blood, bone marrow, and bone samples to measure how bone cells use energy and how bone structure looks. The goal is to better understand the link between mitochondrial disease and bone remodeling disorders.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could reveal how mitochondrial problems affect bone health, pointing toward future treatments for bone disorders.
- What could go wrong
- This is a small, early-stage observational study with only 30 participants. It aims to understand biology, not test a treatment, so direct benefits are unlikely.
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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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2020
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- 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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Accepted
You do not need to have the condition being studied to take part.
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 - cases: * Genetic diagnosis with: MT-TL1 m.3243A\>G, or POLG variant, het or TWNK variant, het, \> 18 years * Signed informed consent Inclusion Criteria - controls: * Healthy subjects matched on age and gender \> 18 years * Signed informed consent Exclusion Criteria: * Renal (creatinine \> 90 µmol/l) * Liver dysfunction (AST \> 3 times the upper limit) * Medical treatment influencing bone metabolism (oral corticosteroid \<12 weeks, anti-osteoporosis treatment, sex steroids, anti-convulsants) * Pregnancy * Excessive consumption of alcohol * Treatment with anticoagulants * Pre-existing coagulopathy * Allergy to lidocaine, morphine or diazepam.
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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
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Dept. of Clinical Genetics
Aalborg, Denmark
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