NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
UMIN ID: UMIN000056776

Registered date:22/01/2025

Test of the Improvement in Bone Density and Secondary Effects of Hydrogen Coral Powder Supplements in Pre-Osteoporosis Cases

Basic Information

Recruitment status Recruiting
Health condition(s) or Problem(s) studiedWomen aged 40 to 75 with pre-osteoporosis
Date of first enrollment2024/10/01
Target sample size10
Countries of recruitmentJapan
Study typeInterventional
Intervention(s)Take five capsules of hydrogen coral powder supplements daily, divided into two doses in the morning and evening

Outcome(s)

Primary OutcomeBone density (femur and lumbar spine)
Secondary OutcomeBlood tests, body composition measurements (height, weight, muscle mass, etc.), and skin frailty-related tests

Key inclusion & exclusion criteria

Age minimum40years-old
Age maximum75years-old
GenderFemale
Include criteria
Exclude criteriaIf the attending physician determines that participation in the trial is inappropriate. History of fractures caused by osteoporosis. Severe diabetes, hypertension, etc. Presence of thyroid disease. Currently taking calcium channel blockers. Due to hypercalcemia as a side effect of vitamin D, blood vitamin D levels and blood calcium levels should be measured and considered.

Related Information

Contact

public contact
Name Koji Yano
Address Rm1008, Kitashinagawa 5-7-14, Shinagawa-ku, Tokyo Japan 141-0001
Telephone 03-5475-8967
E-mail info@suiso1st.co.jp
Affiliation First Co.,Ltd. Clinical Operations Division
scientific contact
Name Koji Yano
Address Rm1008, Kitashinagawa 5-7-14, Shinagawa-ku, Tokyo Japan
Telephone 03-5475-8967
E-mail info@suiso1st.co.jp
Affiliation First Co.,Ltd. Clinical Operations Division