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Calcium From Fish Bone in Volunteers With Osteopenia

Efficacy and Safety of Calcium From Fish Bone in Volunteers With Osteopenia

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05381168
Enrollment
48
Registered
2022-05-19
Start date
2022-05-20
Completion date
2022-12-31
Last updated
2022-05-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteopenia

Keywords

osteopenia, calcium, fish bone, efficacy, safety

Brief summary

The aims of this study are to explore efficacy and safety of calcium from fish bone in volunteers with osteopenia. The volunteers are divided into 2 groups which are calcium from fish bone treatment group and calcium carbonate treatment group. Both groups received the calciums everyday for 6 months. Bone mineral density, blood examination, physical examination, adverse events, and satisfaction are evaluated before and after treatment.

Detailed description

The aims of this study are to explore efficacy and safety of calcium from fish bone in volunteers with osteopenia. The volunteers are divided into 2 groups which are calcium from fish bone treatment group and calcium carbonate treatment group. Both groups received the calciums everyday for 6 months. Bone mineral density is analyzed before and after treatment. Osteocalcin, total procollagen type-1 N-terminal propeptide (P1NP), beta-crosslaps, parathyroid hormone (PTH), calcium, phosphate level, vitamin D level (Serum 25(OH)D), albumin, aspartate transaminase (AST), alanine transaminase (ALT), alkaline phosphatase (ALP), creatinine (Cr), blood urea nitrogen (BUN), and complete blood count (CBC) are assessed before and after taking for 3 and 6 months. Physical performance and food diary are also tested and records. Moreover, adverse effects including skin allergy, gastrointestinal abnormality, respiratory abnormality are evaluated. Satisfaction is asked after treatment.

Interventions

DIETARY_SUPPLEMENTCalcium from fish bone

Calcium from fish bone contained calcium 312 mg and vitamin D 100 IU per capsule.

DIETARY_SUPPLEMENTCalcium carbonate

Calcium carbonate contained calcium 600 mg and vitamin D 200 IU per capsule.

Sponsors

Chulalongkorn University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Intervention model description

The volunteers are divided into 2 groups which are calcium from fish bone treatment group and calcium carbonate treatment group. Both groups receive the calciums every day for 6 months.

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Male age more than 70 years or female age more than 65 years or all age volunteers that have at least 1 risk factors which are menopause before 45 years, menopause with the height reduction (more than 4 cm), body mass index less than 20 kg/mm2, bone fracture history, taking some medicine that has an effect on bone density reduction, have disease that has an effect on bone density reduction, Father and mother have bone fracture history, fracture risk assessment tool (FRAX) in intermediate risk, osteoporosis self-assessment tool for asian (OSTA) score, khon kaen osteoporosis study (KKOS) score in intermediate risk or higher intermediate risk * Bone mineral density between -1 to -2.5 * No osteosclerosis * Can read and write * Willing to be volunteer

Exclusion criteria

* Allergic to calcium, magnesium, phosphorus, zinc, collagen, and osteocalcin * Taking calcium or vitamin D with in 14 days before the study start * Taking osteosclerosis' medicine * Have uncontrolled diseases * Pregnancy and lactation * Participating in other study

Design outcomes

Primary

MeasureTime frameDescription
Bone mineral density score6 monthsBone mineral density score is measured using dual energy x-ray absorptiometry scanner (DEXA scanner). It shows in term of T-score. The outcomes are compared bone mineral density score of calcium from fish bone group to calcium carbonate group.

Secondary

MeasureTime frameDescription
Total procollagen type-1 N-terminal propeptide (P1NP) level6 monthsChanging of P1NP level of calcium from fish bone group compared to calcium carbonate group.
Beta-crosslaps level6 monthsChanging of beta-crosslaps level of calcium from fish bone group compared to calcium carbonate group.
Parathyroid hormone (PTH) level6 monthsChanging of PTH level of calcium from fish bone group compared to calcium carbonate group.
Blood calcium level6 monthsChanging of blood calcium level of calcium from fish bone group compared to calcium carbonate group.
Blood phosphate level6 monthsChanging of blood phosphate level of calcium from fish bone group compared to calcium carbonate group.
Vitamin D level6 monthsChanging of vitamin D level of calcium from fish bone group compared to calcium carbonate group.
Liver function level6 monthsChanging of liver function level (aspartate transaminase (AST), alanine transaminase (ALT), alkaline phosphatase (ALP)) of calcium from fish bone group compared to calcium carbonate group.
Creatinine level6 monthsChanging of creatinine (Cr) level of calcium from fish bone group compared to calcium carbonate group.
Osteocalcin level6 monthsChanging of osteocalcin level of calcium from fish bone group compared to calcium carbonate group.
Pain score6 monthsChanging of pain score using visual analogue scale (0 painless to 10 very pain) of calcium from fish bone group compared to calcium carbonate group.
Short physical performance battery score6 monthsChanging of short physical performance battery score (0 weak to 12 very strong)of calcium from fish bone group compared to calcium carbonate group.
Grip strength6 monthsChanging of grip strength (kilogram) of calcium from fish bone group compared to calcium carbonate group.
Skin allergic reactions6 monthsThe outcome measurements of skin allergic reactions are appearance (have or no have) of rash, edema, bullae, pain, and itching.
Respiratory tract abnormality6 monthsThe outcome measurements of respiratory tract abnormality are appearance (have or no have) of shortness of breath and asthma.
Gastrointestinal tract abnormality6 monthsThe outcome measurements of gastrointestinal tract abnormality are appearance (have or no have) of nausea, vomiting, flatulence, constipation, and diarrhea.
Satisfaction level6 monthsSatisfaction score (0 unsatisfied to 10 very satisfied)
Blood urea nitrogen level6 monthsChanging of blood urea nitrogen (BUN) of calcium from fish bone group compared to calcium carbonate group.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026