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Clinical Trial Summary

Post-menopausal osteoporosis and the resulting fractures are an important cause of disability and loss of independence. They also increase the risk of morbidity and mortality. Given potential side effects, hormone replacement therapy is no longer recommended for menopausal women with risk of becoming osteoporotic. The very significant decrease in the use of these treatments is suspected of contributing to a resurgence in the incidence of osteoporotic fractures, particularly in women before the age of 70. There is a need for prevention of osteoporosis.


Clinical Trial Description

Mother-of-pearl is a candidate for long-term use due to the combination of its effects: calcium supplementation, anti-resorptive activity and osteoanabolic activity. Our hypothesis is that powdered mother-of-pearl supplementation limits bone loss in postmenopausal women with risk of becoming osteoporotic. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05571514
Study type Interventional
Source Centre Hospitalier Universitaire de Saint Etienne
Contact Karima BOUSSOUALIM, MD
Phone (0)4 77 12 76 42
Email karima.Boussoualim@chu-st-etienne.fr
Status Recruiting
Phase N/A
Start date May 12, 2023
Completion date April 2024

See also
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Completed NCT00048061 - MOBILE Study - A Study of Bonviva (Ibandronate) Regimens in Women With Post-Menopausal Osteoporosis Phase 3