Study of the Impact of Mother-of-pearl Nutritional Supplementation on the Prevention of Post-menopausal Osteoporosis
Launched by CENTRE HOSPITALIER UNIVERSITAIRE DE SAINT ETIENNE · Oct 6, 2022
Trial Information
Current as of July 23, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying whether a nutritional supplement made from mother-of-pearl can help prevent osteoporosis in post-menopausal women. Osteoporosis is a condition that weakens bones, making them more likely to break, which can lead to serious health issues and loss of independence. The study aims to find out if this natural supplement can be a safe alternative to hormone replacement therapy, which is no longer recommended for many women due to potential side effects.
To participate in the trial, women aged 50 to 65 who have been through menopause and are at risk for osteoporosis may be eligible. They should have a bone density score (T-score) between -1 and -3 and should not have a history of fractures. However, women with certain medical conditions, such as those affecting bone health or kidney stones, cannot join. Participants can expect to take the supplement and be monitored for its effects on their bone health. This study is important because it explores new ways to help women maintain strong bones after menopause.
Gender
FEMALE
Eligibility criteria
- Inclusion Criteria:
- • Post-menopausal women (50-65y) with risk of becoming osteoporotic
- • T-score between -1 and -3
- • Absence of fragility fractures history
- Exclusion Criteria:
- • absence of parathyroid glands (phospho-calcic regulation)
- • presence of kidney stones
- • patients who follow a treatment that could interfere with bone metabolism (corticotherapy, menopausal hormonal therapy, anti-oestrogen treatment, non-controlled hyperthyroiditis, hyper- and hypothyroiditis)
- • bone diseases (Paget'disease, osteomalacia)
- • chronic alcoholism
About Centre Hospitalier Universitaire De Saint Etienne
The Centre Hospitalier Universitaire (CHU) de Saint-Étienne is a leading academic medical center in France, dedicated to advancing healthcare through innovative clinical research and high-quality patient care. With a robust infrastructure that supports a wide range of medical specialties, CHU de Saint-Étienne fosters collaboration between healthcare professionals, researchers, and academic institutions. The center is committed to conducting rigorous clinical trials that adhere to ethical standards and regulatory requirements, aiming to improve treatment outcomes and enhance the overall health of the community. Through its dedication to scientific excellence and patient-centered care, CHU de Saint-Étienne plays a pivotal role in the advancement of medical knowledge and the development of new therapeutic interventions.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Lyon, , France
Paris, , France
Clermont Ferrand, , France
Roanne, , France
Saint étienne, , France
Le Puy En Velay, , France
Grenoble, , France
Patients applied
Trial Officials
Adamah AMOUZOUGAN, MD
Principal Investigator
CHU SAINT-ETIENNE
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Similar Trials