Fish bones may fortify Women's bones: new study
NCT ID NCT05066477
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tested whether a supplement made from salmon bone powder (CalGo) could help prevent bone loss in perimenopausal women with low bone density. Eighty women aged 50 and older took either the supplement or a placebo for up to 24 months. Researchers measured changes in bone density at the hip, spine, and forearm to see if the supplement slowed bone thinning.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- salmon bone meal (CalGo) with vitamin D3
- What this could lead to
- If it works, this could provide a natural dietary supplement to help maintain bone density in women at risk for osteoporosis.
- What could go wrong
- This is a small, completed trial with 80 participants. The supplement may not significantly slow bone loss, and results may not apply to all women.
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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80 people
The number who actually took part.
- Started
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Sep 2021
- Finished
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Jun 2025
- Lead sponsor
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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.
- Ages
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50 years and older
- Sex
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Female participants only
- 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: * Female gender * ≥ 50 years of age * DXA T-score of \> -2.5 standard deviations, but ≤ -1 (osteopenic range) * Steady state body weight 1 month before study commencement date * No contraindications for intake of the interventional product, including a prior diagnosis of fish allergy. * Familiar with the Norwegian language, both in writing and orally Exclusion Criteria: * A diagnosis of osteoporosis (BMD T-score ≤ -2.5 SD as diagnosed by DXA), or any previously diagnosed fragility fractures on a background of osteoporosis. * Use of drugs known to affect bone metabolism, including: * Glucocorticoids * Thyroid hormones * Hormone replacement therapy taken continuously for a duration of less than 6 months. * Long-term heparin therapy * Anti-convulsive drugs * Long-term proton pump inhibitor treatment * Lithium * Anti-osteoporotic drugs * Cancer therapy * Selective estrogen receptor modulators. * Any disease or medical condition known to affect bone tissue, including neoplasia with or without metastasis, Paget's disease of bone, Osteomalacia, or any other disease deemed relevant by the PI. * Gastrointestinal diseases or disturbances potentially affecting absorption of nutrients, including Crohn's disease and Celiac disease. * Hypersensitivity to ingredients in the interventional product, including fish allergy. * Not willing to participate in the study. * Other reasons that the PI deems it necessary to exclude the subject.
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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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Hofseth Biocare ASA
Ålesund, Møre og Romsdal, 6005, Norway
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Kristiansund Hospital
Kristiansund, Møre og Romsdal, 6508, Norway
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Lovisenberg Diakonale Sykehus
Oslo, 0456, Norway
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