Clinical TrialID 8042

Effects of Amorphous Calcium Carbonate Supplementation on Bone Health in Postmenopausal Women With Osteopenia

NCT05810909

Calcium|Osteopenia|Bone Mineral Density|Bone Turnover Marker

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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
8042
Evidence Id
8042
Core Evidence Id
8042
Source Clinical Trial Id
8038
Herb2 Clinical Trial Id
HBCT008038
Nct Id
NCT05810909
Title
Effects of Amorphous Calcium Carbonate Supplementation on Bone Health in Postmenopausal Women With Osteopenia
Status
Completed
Phase
Study Result
No
Study Condition
Calcium|Osteopenia|Bone Mineral Density|Bone Turnover Marker
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: QUADRUPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: PREVENTION
Intervention
DIETARY_SUPPLEMENT: amorphous calcium carbonate/ Placebo
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Quadruple
Intervention Purpose
Prevention
Gender
Female
Age
Child, Adult, Older_Adult
Enrollment
35
Outcome Measure
bone density change, monitoring bone mineral density change and bone turnover markers change, 6 months
Sponsor Collaborator
Universal Integrated Corp.|Taipei Medical University
Funded By
INDUSTRY
Location
Taipei Medical University, Taipei, 110, Taiwan
Other Id
N201912029
Start Date
2019-12-10
Primary Completion Date
2021-12-10
Completion Date
2022-09-22
First Posted
2023-04-13
Results First Posted
Last Update Posted
2023-04-13
Study Document
Study Url
https://clinicaltrials.gov/study/NCT05810909
Title Cn
Title En
Effects of Amorphous Calcium Carbonate Supplementation on Bone Health in Postmenopausal Women With Osteopenia
Bilingual Status
semi_complete