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Vitamins D and K Effects on Vascular Function in Obese Adults.

Primary Purpose

Obesity, Vitamin D3 Deficiency

Status
Recruiting
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Vitamin D3 + K2-MK7
Placebo
Vitamin D3
Sponsored by
Hospital Universitario Pedro Ernesto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity focused on measuring Obesity, Vitamin D3 Deficiency, Vitamin K, Sympathetic tonus, Endothelial dysfunction, Arterial stiffness

Eligibility Criteria

40 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Vitamin D deficiency; Vitamin D insufficiency; Obesity; Overweight; Exclusion Criteria: Diabetes mellitus; Arterial coronary disease; Beta blocker use; cancer; ESRD;

Sites / Locations

  • Rio de Janeiro State UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Placebo Comparator

Active Comparator

Experimental

Arm Label

Placebo

Vitamin D3

Vitamin D3 + K2-MK7

Arm Description

Placebo - Medium-chain triglyceride

Vitamin D3 - 7000 IU daily

Vitamin D3 - 7000 IU + Vitamin K2-MK7 180mcg combined, daily

Outcomes

Primary Outcome Measures

Microvascular reactivity
A laser speckle contrast imaging system with a laser wavelength of 785 nm system will measure non-invasively real time cutaneous microvascular flow changes in the forearm. For the post occlusive reactive hyperemia test, arterial occlusion will be performed with suprasystolic pressure (50 mmHg above the systolic arterial pressure) using a sphygmomanometer applied to the arm of the subject over three minutes. Peak skin flow will be measured after pressure release.

Secondary Outcome Measures

Central blood pressure
Central systolic blood pressure, diastolic blood pressure, mean arterial pressure and pulse pressure before and after intervention and their potential effects on changes in subendocardial viability ratio and ejection duration after intervention with beetroot juice and water.

Full Information

First Posted
January 10, 2023
Last Updated
January 10, 2023
Sponsor
Hospital Universitario Pedro Ernesto
Collaborators
Rio de Janeiro State Research Supporting Foundation (FAPERJ), Conselho Nacional de Desenvolvimento Científico e Tecnológico
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1. Study Identification

Unique Protocol Identification Number
NCT05689632
Brief Title
Vitamins D and K Effects on Vascular Function in Obese Adults.
Official Title
Effects of Vitamin D3 and Vitamin K2MK7 Supplementation on Vascular Function in Overweight or Obese Adults.
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 15, 2022 (Actual)
Primary Completion Date
July 15, 2023 (Anticipated)
Study Completion Date
November 15, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Universitario Pedro Ernesto
Collaborators
Rio de Janeiro State Research Supporting Foundation (FAPERJ), Conselho Nacional de Desenvolvimento Científico e Tecnológico

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
A prospective, randomized, placebo-controlled, double-blind study that aims to evaluate the effects of combined vitamin D3 and K2-MK7 supplementation on vascular function, sympathetic tone, metabolic biomarkers and inflammatory factors in a population of overweight or obese adults and deficient or insufficient serum levels of vitamin D.
Detailed Description
Overweight and obesity are public health issues of epidemic proportions nowadays. They constitute risk factors for several chronic diseases with vascular, metabolic, and inflammatory changes. Adequate serum levels of vitamin D are correlated with good cardiovascular and metabolic health, since its deficiency and insufficiency (highly prevalent in obesity) have an inverse correlation. Likewise, vitamin K, especially K2, is related to the reduction of arterial stiffness, suppression of the inflammation in the vascular wall, favorable action on the lipid profile, whereas insufficiency is related to increased cardiovascular risk. The combined use of vitamin D and K aiming to reduce cardiovascular risk has been studied, however, the results of randomized clinical trials are still controversial. This prospective, randomized, placebo-controlled, double-blind trial aims to evaluate the effect of supplementation of vitamins D3 and K2-MK7 on vascular function, sympathetic tone, metabolic biomarkers and inflammatory factors in a population of overweight or obese adults and serum levels of deficient or insufficient vitamin D. Individuals of both sexes, aged between 40 and 70 years, body mass index (BMI) ≥ 25 and < 40 kg/m² and vitamin 25OHD3 <30 ng/ml will be randomized into 3 groups (A/B/C) to receive supplementation (Placebo/VitD3 7000 IU/VitD3 7000IU+K2-MK7-180mcg) daily for 16 weeks. Individuals will be rated at 4 visits namely: V0 screening according to inclusion and exclusion criteria; clinical, anthropometry and electrical bioimpedance, laboratory and vascular evaluation before supplementation; V1 supplementation begins; V2 after 8 weeks; V3 at the end of the intervention. The laboratory evaluation consists of blood count, biochemistry, electrolytes, glucose, lipid, liver and thyroid profiles, vitamin D3 and parathyroid hormone, in addition to the urinary excretion of calcium and creatinine. Sympathetic tone is assessed by a frequency meter (Polar® Verity Sense), arterial stiffness by measuring the pulse wave velocity by oscillometry (Mobil-O-Graph®) and endothelium function by measuring post-occlusion microvascular reactivity using laser speckle contrast image-LSCI.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Vitamin D3 Deficiency
Keywords
Obesity, Vitamin D3 Deficiency, Vitamin K, Sympathetic tonus, Endothelial dysfunction, Arterial stiffness

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Prospective, randomized, placebo-controlled, double-blind study
Masking
Outcomes Assessor
Masking Description
The participants and the investigator do not know which supplements are taken.
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo - Medium-chain triglyceride
Arm Title
Vitamin D3
Arm Type
Active Comparator
Arm Description
Vitamin D3 - 7000 IU daily
Arm Title
Vitamin D3 + K2-MK7
Arm Type
Experimental
Arm Description
Vitamin D3 - 7000 IU + Vitamin K2-MK7 180mcg combined, daily
Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin D3 + K2-MK7
Intervention Description
Combined supplementation
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
MCT
Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin D3
Intervention Description
Vitamin D3 - 7000 IU
Primary Outcome Measure Information:
Title
Microvascular reactivity
Description
A laser speckle contrast imaging system with a laser wavelength of 785 nm system will measure non-invasively real time cutaneous microvascular flow changes in the forearm. For the post occlusive reactive hyperemia test, arterial occlusion will be performed with suprasystolic pressure (50 mmHg above the systolic arterial pressure) using a sphygmomanometer applied to the arm of the subject over three minutes. Peak skin flow will be measured after pressure release.
Time Frame
150 minutes
Secondary Outcome Measure Information:
Title
Central blood pressure
Description
Central systolic blood pressure, diastolic blood pressure, mean arterial pressure and pulse pressure before and after intervention and their potential effects on changes in subendocardial viability ratio and ejection duration after intervention with beetroot juice and water.
Time Frame
150 minutes

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Vitamin D deficiency; Vitamin D insufficiency; Obesity; Overweight; Exclusion Criteria: Diabetes mellitus; Arterial coronary disease; Beta blocker use; cancer; ESRD;
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Adriana C Faria, MD
Phone
5521999834054
Email
afmenie@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Mario F Neves, MD, PhD
Email
mariofneves@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adriana C Faria, MD
Organizational Affiliation
State University of Rio de Janeiro
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mario F Neves, MD, PhD
Organizational Affiliation
State University of Rio de Janeiro
Official's Role
Study Director
Facility Information:
Facility Name
Rio de Janeiro State University
City
Rio de Janeiro
ZIP/Postal Code
20551-030
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Adriana C Faria, MD
Phone
5521999834054
Email
afmenie@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
No plans to share IPD with other researchers

Learn more about this trial

Vitamins D and K Effects on Vascular Function in Obese Adults.

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