Clinical Trials Directory

Trials / Completed

CompletedNCT03146273

Study of Absorption Characteristics of Two Multivitamin Mineral Formulations (Gel vs. Tablet/Capsule)

A Pharmacokinetic Crossover Comparison Study of Absorption Characteristics of Two Multivitamin Mineral Formulations (Gel vs. Tablet/Capsule)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Galilee CBR · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

This clinical study is designed to evaluate difference in the AUC of the absorption of Multivitamin and minerals defined in the protocol

Detailed description

This clinical study is designed to evaluate difference in the AUC of the absorption of Multivitamin and minerals: 1. Tablet/capsule administration - up to 20 healthy volunteers will be recruited to the study. The tablet/capsule will be administered as a single dose after 12 hours of fasting. The participants will be monitored during 6 hours for the level of minerals and Multivitamin minerals in the blood, adverse events and vital signs. 2. Gel administration - the gel will be administrated to the same group of patients in the single dose after 12 hours of fasting. The participants will be monitored during 6 hours for the level of minerals and Multivitamin minerals in the blood, adverse events and vital signs.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTMultivitaminsAfter the study product administration blood tests will be performed in order to calculate the AUC for each mineral and vitamin - Vit A Vit E Folic Acid Vit C Calcium Magnesium After the washout period, the same procedure will be done for the additional formulation of the multivitamins.

Timeline

Start date
2017-05-09
Primary completion
2017-06-10
Completion
2017-07-01
First posted
2017-05-09
Last updated
2024-09-26

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT03146273. Inclusion in this directory is not an endorsement.