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Evaluation of changes in serum magnesium concentrations following oral administration of different magnesium salts

Evaluation of changes in serum magnesium concentrations following oral administration of different magnesium salts - Evaluation of changes in serum magnesium concentrations following oral administration of different magnesium salts

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000061032
Enrollment
10
Registered
2026-03-30
Start date
2026-03-30
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy adults

Interventions

Take 2000mg capsule containing magnesium derived from rice bran (containing 300mg of magnesium) one time. Take 1746mg capsule containing magnesium phosphate, tribasic (containing 300mg of magnesium) o

Sponsors

Tsuno Rice Fine Chemicals Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Healthy individuals in their 20s to 40s. 2. Healthy individuals without chronic physical illnesses, as confirmed through medical interviews. 3. Individuals not consuming any food products with fatigue-recovery effects. 4. Individuals who have received sufficient explanation regarding the purpose and content of this trial, possess the capacity to consent, voluntarily volunteer to participate after fully understanding the details, and can provide written consent to participate in this trial. 5. Individuals who can attend the designated examination date and undergo the examination. 6. Individuals deemed suitable for participation in this trial by the principal investigator.

Exclusion criteria

Exclusion criteria: 1. Individuals currently suffering from any disease and undergoing drug therapy. 2. Individuals with severe disease symptoms such as motor dysfunction or respiratory disorders. 3. Individuals unable to refrain from taking over-the-counter magnesium supplements during the trial period. 4. Individuals with allergies (to pharmaceuticals or trial-related products). 5. Individuals who are pregnant, breastfeeding, or intend to become pregnant during the trial period. 6. Individuals who currently have, or have had within the past month, a habit of continuously taking or applying medications specifically marketed for magnesium fortification or supplementation. 7. Individuals using potent pharmaceuticals (as determined by the principal investigator). 8. Other individuals deemed unsuitable for this trial by the principal investigator.

Design outcomes

Primary

MeasureTime frame
Plasma magnesium concentration

Secondary

MeasureTime frame
Post-Consumption Health Questionnaire

Countries

Japan

Contacts

Public ContactYuki Inoue

Tsuno Rice Fine Chemicals Co., Ltd. Section II. Planning and Deveropment Dept 3. Research and Development Div.

inoue.yuki@tsuno.co.jp0736-26-5032

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026