Calcium Absorption and Retention From Marine Products
|ClinicalTrials.gov Identifier: NCT00393289|
Recruitment Status : Completed
First Posted : October 27, 2006
Last Update Posted : July 20, 2016
|Condition or disease||Intervention/treatment||Phase|
|Calcium Metabolism||Behavioral: Calcium controlled diet||Not Applicable|
Hide Detailed Description
Up till now little attention has been given the exploitation of marine by-products from the fishing industry. Calcium in fish is found mainly in bone and skin. By-products from these sources are limited to production of gelatine. Small fish, which can be eaten whole with bones included, are traditionally considered to be a good source of calcium. Until recently, bioavailability of this calcium was not known. Two recent studies from Denmark have shown that the absorption of calcium from small soft-boned fish was comparable to that of skimmed milk both in rats and in humans.
Calcium fortified foods are likely to play an important role in helping consumers to achieve calcium requirements aimed at reducing the risk of developing osteoporosis. Experimental evidence show a positive effect of calcium supplementation on bone mineral accretion in children, and combined calcium and vitamin D supplementation has resulted in reduced bone loss and fracture incidence in older men and women.
This protocol describes a project on the nutritional utilisation of calcium from fish bone waste. The main objective is to maximise the use and the added value of marine by-products with special emphasis on utilisation of fish bone as a calcium source and determine its bioavailabiliy in humans.
Study design :
This study will follow a 3x7 weeks ransomised crossover design, where the calcium absorption and retention will be measured form meals labelled with 47Ca. The test meals will be digested in the morning after a 12h fast and bloodsampling. Whole body retention will be measured on day 15, 22 and 26, and calibrated against a background measurement from the day prior to ingestion of the test meal. The subjects will receive an ordinary standardised diet for 2 days prior and 3 days after the test meals. This diet will be standardised to match the subjects' individual calcium intake.
Two types of fish bone meal (from salmon and cod fish) and a control (CaCO3) will be tested. Amounts equivalent of 800 mg Ca will be baked into bread, which will be labelled with 47Ca and served with 500 mL of ultra pure water at the department.
Isotopes and labelling procedure:
Isotopes (47Ca) will be ordered from Risø National Laboratory, Radiation Research Department, Denmark. The department of Human Nutrition will recieve the prepared doses of isotopes the day before the test meal. A dose of 0.2 MBq/ml will be used. The doses will be used to extrinsically label the test meals by drop-wise adding 1 ml of isotope solution in the afternoon on the day before intake of test meals and stored at 5 degree C until ingested.
Since each subject will recieve labelled meals on three occasions, a total dose of 0.6 MBq will be ingested during the study.
Measurement of calcium retention:
The whole body retention of calcium will be measured with a whole body counter at the Copenhagen University Hospital, Denmark. All measurements of calcium retention will be corrected for physical decay back to the time of administration.
Serun calcium, phosphorus and vitamin D concentrations will be determined in before each test meal. Plasma levels of PTH will be determined before the first test meal only.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||12 participants|
|Intervention Model:||Crossover Assignment|
|Masking:||Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|
|Primary Purpose:||Basic Science|
|Official Title:||Calcium Absorption and Retention From Marine Products|
|Study Start Date :||November 2005|
|Actual Primary Completion Date :||April 2006|
|Actual Study Completion Date :||March 2007|
- Whole body retention of calcium
- D-vitamin and PTH status, serum calcium and phosporus, and calcium intake
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00393289
|Institute of Human Nutirtion, The Royal Veterinary and Agricultural University, Denmark|
|Frederiksberg, Frederiksberg C, Denmark, 1958|
|Principal Investigator:||Susanne Bügel, MSc, PhD||Institute of Human Nutrition, THe Royal Veterinary and Agricultural University, Denmark|