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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03471481
Other study ID # 150003722
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date August 10, 2015
Est. completion date August 1, 2019

Study information

Verified date November 2019
Source Drexel University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The objective of this study is to determine the role of magnesium on bone and vitamin D metabolism in patients receiving anti-epileptic medications.


Recruitment information / eligibility

Status Terminated
Enrollment 7
Est. completion date August 1, 2019
Est. primary completion date August 1, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Individuals receiving anti-epileptic drugs as a treatment for epilepsy Exclusion Criteria: - Individuals who are pregnant or breastfeeding, receiving cancer treatments, have liver or kidney diseases, autoimmune diseases, or other diseases that may interfere with vitamin D and magnesium metabolism.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
No Intervention. Study is Cross Sectional in nature
No Intervention. Study is cross sectional in nature

Locations

Country Name City State
United States Drexel University Philadelphia Pennsylvania
United States Drexel University Nutrition Sciences Research Lab Philadelphia Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Drexel University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Bone mineral density Will be measured at Tibia, Hip and Total Body using a DXA scan 1 time point - baseline
Secondary Ionized Magnesium in serum This will be assayed in the serum 1 time point - baseline
Secondary Vitamin D - 25 hydroxy vitamin D This will be assayed in the serum 1 time point - baseline
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