Skip to main content
MedPathMedPath Home
Clinical Trials/CTRI/2023/05/052693
CTRI/2023/05/052693
Not yet recruiting
未知

Bone mineral changes in response to increasing dietary calcium intake in children, a study to assess thenatural variability of urinary isotopes of calcium.

The New York Academy of Sciences.0 sites0 target enrollmentTBD
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
The New York Academy of Sciences.
Status
Not yet recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
The New York Academy of Sciences.

Eligibility Criteria

Inclusion Criteria

  • •Healthy children between 6 to 10 years old. Vitamin D 25OHD ( \> 20ng/mL). Non\-anaemic Hb \>11\.5\.0 g/dL. Z score \>\- 2SD. Not taking any food supplements/fortified drinks. Not planning to move out during the study duration.

Exclusion Criteria

  • •Age: \<6 and \>10 years Severe anemia (Hb \<8g/dl) Severely malnourished children with weight for height Z score \< \-3SD Any food allergy or food intolerance Any metabolic, gastrointestinal kidney or chronic diseases such as diabetes, hepatitis, hypertension, cancer, or cardiovascular diseases (according to the participant’s statement) Continuous/long\-term use of medication during the whole study Consumption of mineral and vitamin supplements within 2 weeks before the start of the study Blood transfusion, blood donation or significant blood loss (accident, surgery) over the past 4 months Earlier participation in any clinical study within the last 30 days A participant who cannot be expected to comply with the study protocol (e.g., not available on certain study appointments) Likely to move out of the study area within the period of the study intervention. Difficulties with blood samplinG.

Outcomes

Primary Outcomes

Not specified

Similar Trials

Completed
Not Applicable
Bone mineral density changes from view points of exercise and dietadult femalere
JPRN-UMIN000047928Suzuka University of Medical Science18
Completed
Not Applicable
The Effect on Behavior and Bone Mineral Density of Individualized Bone Mineral Density Feedback and Educational Interventions in Premenopausal Women: a Randomized Controlled Trial.
ACTRN12605000139673niversity of Tasmania400
Recruiting
Not Applicable
A prospective study of bone mineral density changes in patients during perioperative chemotherapy for breast cancerBreast cancer
JPRN-UMIN000053265Hyogo Prefectural Harima Himeji General Medical Center50
Completed
Not Applicable
Effect on bone turnover and Bone Mineral Density (BMD) of low dose oral silicon as an adjunct to calcium/vitamin D3 in a randomised, placebo-controlled trial
ISRCTN57103074Bio Minerals N.V. (Belgium)184
Active, not recruiting
Phase 1
Changes in bone density and bone turnover in patients with rheumatoid arthritis treated with rituximab, a B cell depleting monoclonal antibody.An investigator-led, industry supported, multicentre, open-label, single treatment arm, prospective clinical trial. - Effects of B cell depletion on bone turnover in rheumatoid arthritis.
EUCTR2010-020499-50-GBSouth Tees Hospitals NHS Foundation Trust46