A Clinical Trial Investigating the Effect of Salmon Bone Meal on Bone Mass Among Osteopenic Women

A Randomized, Double-blind Clinical Trial Investigating the Efficacy of Salmon Bone Meal on Bone Mineral Density Among Perimenopausal Osteopenic Women

The purpose of this study is to evaluate the efficacy of salmon bone meal in preventing bone loss among perimenopausal women with reduced bone mass density.

Study Overview

• Status: Active, not recruiting
• Conditions: Osteopenia; Osteopenia of the Elderly
• Intervention / Treatment: Dietary supplement: CalGo; Other: Placebo

Detailed Description

The current study is part of a larger project called the CalGo-project. The overall purpose of the study is to use bone meal from salmon to promote skeletal health. Specifically, the effect of salmon bone meal on bone mass density among perimenopausal women (age ≥ 50 years) with osteopenia is investigated over a time period of 2 years. Salmon bone meal is composed of a natural microcrystalline hydroxyapatite form of calcium and phosphorus, collagen type 2. Past literature on mammalian sources of bone meal has indicated that this form of calcium is superior in terms of preserving bone mass density compared to traditional calcium supplements. Preserving bone mass is essential to reduce the risk of future fragility fractures. Osteopenia is a condition of reduced bone mass density and bone quality which can indicate the later onset of clinical osteoporosis. Both are conditions associated with a significant risk of fragility fractures, which are a major global health burden.

Bone mass density is measured using dual-energy X-ray absorptiometry. Markers of bone formation P1NP and CTX-1 will be measured in serum samples of participants. 100 potential participants will be screened for eligibility. Participants who meet the eligibility criteria will be randomized in a double-blind manner to receive 4 capsules daily of salmon bone meal enriched with Vitamin D3 per capsule.

• Study Type: Interventional
• Enrollment (Actual): 80
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Erland Hermansen, MD, PhD; Phone Number: 0047 915 13 690; Email: ehe@hofsethbiocare.no
• Study Contact Backup: Name: Anne R Standal, MSc; Phone Number: +4740016800; Email: forskning@hofsethbiocare.no

Study Locations

• Norway
  • Oslo, Norway, 0456
    • Lovisenberg Diakonale Sykehus
  • Møre Og Romsdal
    • Kristiansund, Møre Og Romsdal, Norway, 6508
      • Kristiansund Hospital
    • Ålesund, Møre Og Romsdal, Norway, 6005
      • Hofseth Biocare ASA

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 50 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes

Description

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.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Prevention
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Triple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: CalGo (Salmon bone meal); 4 capsules daily of CalGo (salmon bone meal enriched with Vitamin D3) is taken per orally. Each capsule contains ~500 mg of salmon bone meal (380 mg calcium, 200 mg phosphorus, 500 mg native collagen type 2), and 10 micrograms of vitamin D3 (400 IU). Once daily dosing. Duration: 2 years.	Dietary supplement: CalGo; CalGo is a natural marine collagenic bone powder from salmon. The bone powder is a 100 % microcrystalline hydroxyapatite form of calcium and phosphorus. Furthermore it contains collagen type 2 and is enriched with vitamin D3.
Placebo Comparator: Maltodextrin; 4 capsules daily of maltodextrin is taken per orally. Each capsule contains 500 mg of maltodextrin. Once daily dosing. Duration: 2 years.	Other: Placebo; Pure maltodextrin

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Mean change in Bone Mass Density (BMD) of the femoral neck at Month 12, and Month 24.	Change in BMD of the femoral neck is assessed based on dual-energy X-ray absorptiometry T-scores.	Baseline, 12 Months, and 24 Months.

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Mean change in Bone Mass Density (BMD) of the lumbar spine (L1-L4) at Month 12, and Month 24.	Change in BMD of the lumbar spine segments L1-L4 is assessed based on dual-energy X-ray absorptiometry T-scores.	Baseline, 12 Months, and 24 Months
Mean change in Bone Mass Density (BMD) of the distal forearm at Month 12, and Month 24.	Change in BMD of the distal forearm (distal radius) is assessed based on dual-energy X-ray absorptiometry T-scores.	Baseline, 12 Months, and 24 Months
Change in serum levels of markers of bone formation at Month 6, Month 12, and Month 24.	Serum markers of bone formation are analyzed in frozen serum samples from participants.	Baseline, 6 Months, 12 Months, and 24 Months.
Change from Baseline in self-assessed quality of life on the EuroQol-5 Dimensions-3 Levels (EQ-5D-3L) instrument at Month 24.	5Q-5D-3L is a standardized instrument used to measure generic quality of life based on five distinct dimensions. EQ-5D-3L contains two parts. The first part contains five questions that the individual must answer and includes mobility (walking), self-care, usual activities, pain/discomfort, and anxiety/depression. For each item, there are three possible answers. Results are reported as a five-digit number ranging from 11111 (best health status) to 33333 (worst health status). Several methods exist for analysing these number profiles, and it is possible to convert the number profile into an index number. The second part is the EQ-VAS, where the patient self-assesses their overall health on a visual analogue scale (VAS), with 100 indicating the best health status.	Baseline and 24 Months
Difference in number of Adverse Events between the study groups.	To assess whether there is a statistically significant difference in the number of adverse events between the two study groups (CalGo [Salmon Bone Meal] and Placebo).	3 Months, 6 Months, 12 Months, 18 Months, 24 Months
Difference in number of fractures between the two study groups.	To assess whether there is a statistically significant difference in the number of fractures between the two study groups (CalGo [Salmon Bone Meal] and Placebo).	3 Months, 6 Months, 12 Months, 18 Months, 24 Months
Difference in urine calcium in a spot urine sample between the two study groups.	Amount of calcium will be measured in spot urine samples from participants.	Baseline, 12 Months, and 24 Months.

Collaborators and Investigators

• Sponsor: Hofseth Biocare ASA
• Collaborators: Møre og Romsdal Hospital Trust
• Investigators: Principal Investigator: Øystein B Lian, MD, PhD, Møre og Romsdal Hospital Trust (Helse Møre og Romsdal), Kristiansund Hospital

Study record dates

Study Major Dates

• Study Start (Actual): September 22, 2021
• Primary Completion (Estimated): July 3, 2025
• Study Completion (Estimated): July 3, 2025

Study Registration Dates

• First Submitted: September 22, 2021
• First Submitted That Met QC Criteria: October 1, 2021
• First Posted (Actual): October 4, 2021

Study Record Updates

• Last Update Posted (Actual): September 26, 2023
• Last Update Submitted That Met QC Criteria: September 25, 2023
• Last Verified: September 1, 2023

More Information

Terms related to this study

• Keywords: bone mineral density; bone mass; bone meal; bone mass density; salmon bone meal
• Additional Relevant MeSH Terms: Metabolic Diseases; Musculoskeletal Diseases; Bone Diseases; Bone Diseases, Metabolic
• Other Study ID Numbers: CALGO-OST

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No