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Omega 3 and Vitamin D Dosage in a Population With Moderate to High Risk of AMD (OVID-AMD)

Primary Purpose

Age-related Macular Degeneration, Vitamin D Deficiency

Status
Completed
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
blood sample
Sponsored by
Universitaire Ziekenhuizen KU Leuven
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Age-related Macular Degeneration focused on measuring micronutrients

Eligibility Criteria

55 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • age over 55
  • STARS score > or = 10 (moderate to high risk for AMD)

Exclusion Criteria:

  • STARS score < 10
  • persons taking nutritional supplements containing vitamin D or trace nutrients in the 4 months prior to enrollment
  • persons with grade-3 or grade-4 AMD scores according to the AREDS simplified scale

Sites / Locations

  • UZLeuven

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

pilot study 1 arm

Arm Description

50 subjects with no AMD or early AMD, aged over 55, at moderate-to-high risk for AMD based on a simplified AMD risk assessment scale score > or = 10, not taking vitamin D or trace nutriënt containing supplements

Outcomes

Primary Outcome Measures

concentration of vitamin D
vitamin D deficiency

Secondary Outcome Measures

concentration of fatty acids
omega 6/omega 3 ratio, DHA, EPA
concentration of zinc oxide
in µg/L

Full Information

First Posted
July 7, 2020
Last Updated
July 17, 2020
Sponsor
Universitaire Ziekenhuizen KU Leuven
Collaborators
Laboratoires Thea
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1. Study Identification

Unique Protocol Identification Number
NCT04482465
Brief Title
Omega 3 and Vitamin D Dosage in a Population With Moderate to High Risk of AMD
Acronym
OVID-AMD
Official Title
Omega 3 and Vitamin D Dosage in a Population With Moderate to High Risk of Age-related Macular Degeneration
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
April 20, 2017 (Actual)
Primary Completion Date
October 5, 2017 (Actual)
Study Completion Date
October 5, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universitaire Ziekenhuizen KU Leuven
Collaborators
Laboratoires Thea

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Objectives: The investigators conducted a prospective study in Belgium with the objective to determine the proportion of subjects identified at moderate-to-high risk for AMD, based on the STARS® questionnaire, in need of nutritional supplementation by assessing their vitamin D, zinc oxide and fatty acid profile status. Methods: This multicentre epidemiological intervention pilot study involved 50 Belgian subjects with no AMD or early AMD, aged over 55, at moderate-to-high risk for AMD based on a simplified AMD risk assessment scale (STARS®) score ≥ 10, not taking vitamin D or trace nutrient containing supplements. Outcome data was collected during a one-time subject interview comprising of clinical eye examinations (typically visual acuity), the STARS® questionnaire, visual acuity assessment, an OCT scan on the macula, and fundus photography. Blood samples were collected from the patients and serum analysis was performed to determine the levels of omega-6 to omega-3 ratio, EPA and DHA, zinc and cupric oxide, and vitamin D, recognised as key nutrients involved in AMD pathophysiology.
Detailed Description
Study population This pilot study is a multicentre epidemiological intervention study of exploratory nature, hence no power calculation was performed, aiming to demonstrate trends. The study includes 50 subjects without a control group. The inclusion criteria of the 50 subjects are: people over 55 years old, with a STARS® score ≥10 (moderate-to-high risk for AMD). Individuals with a STARS® score <10, or taking nutritional supplements containing vitamin D or trace nutrients in the 4 months prior to enrolment, and people with grade-3 or grade-4 AMD scores according to the AREDS simplified scale, were excluded from the study. Study Design and Procedures The study was conducted in accordance to the GCP and Declaration of Helsinki principles, and the study protocol and all relevant study documents were submitted for review to the UZ Leuven Ethics Committee. Informed consent form was obtained from the subjects prior to their enrolment in the study. All information collected was kept confidential and anonymized and used exclusively for the purposes of this study in compliance with the applicable personal data protection and processing laws. The study was completed within a single visit. Outcome data was collected during a one-time subject interview comprising of clinical eye examinations (typically visual acuity), the STARS® questionnaire, visual acuity assessment, an OCT scan on the macula, and fundus photography. Blood samples were collected using a Vacutainer system with 1 purple EDTA tube and 2 red tubes to assay for omega-3 fatty acids, EPA and DHA as well as omega-6 for the calculation of the omega-6:omega-3 (Ω6:Ω3) ratio, vitamin 25(OH)D, zinc oxide and cupric oxide. Samples were analysed by the RP Lab, Rue Emile Francqui 7, 1435 Mont-Saint-Guibert, Belgium (www.rplab.be). Data Analysis The data were tested for normality using the Chi-Squared Goodness-of-Fit test. Data distribution was not normal for some of the assayed micronutrients, thus all data were analysed to identify trends using subject proportions (%) and descriptive statistics for not normally distributed data: median ± MAD (median absolute deviation).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Age-related Macular Degeneration, Vitamin D Deficiency
Keywords
micronutrients

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
epidemiological intervention pilot study
Masking
None (Open Label)
Masking Description
blood results were communicated to each participant
Allocation
N/A
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
pilot study 1 arm
Arm Type
Other
Arm Description
50 subjects with no AMD or early AMD, aged over 55, at moderate-to-high risk for AMD based on a simplified AMD risk assessment scale score > or = 10, not taking vitamin D or trace nutriënt containing supplements
Intervention Type
Diagnostic Test
Intervention Name(s)
blood sample
Intervention Description
blood sample to determine omega6/omega 3 ratio, EPA, DHA, zinc, cupric oxide, vitamine D
Primary Outcome Measure Information:
Title
concentration of vitamin D
Description
vitamin D deficiency
Time Frame
at the time of the procedure
Secondary Outcome Measure Information:
Title
concentration of fatty acids
Description
omega 6/omega 3 ratio, DHA, EPA
Time Frame
at the time of the procedure
Title
concentration of zinc oxide
Description
in µg/L
Time Frame
at the time of the procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age over 55 STARS score > or = 10 (moderate to high risk for AMD) Exclusion Criteria: STARS score < 10 persons taking nutritional supplements containing vitamin D or trace nutrients in the 4 months prior to enrollment persons with grade-3 or grade-4 AMD scores according to the AREDS simplified scale
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Julie Jacob, MD PhD
Organizational Affiliation
Universitaire Ziekenhuizen KU Leuven
Official's Role
Principal Investigator
Facility Information:
Facility Name
UZLeuven
City
Leuven
ZIP/Postal Code
3000
Country
Belgium

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
results will be published
Citations:
PubMed Identifier
33620690
Citation
Jacob J, Mangelschots E, Michez M, Sanak SN, Leys A. Cross-Sectional Study on Vitamin D, Zinc Oxide and Fatty Acid Status in a Population with a Moderate to High Risk of AMD Identified by the STARS(R) Questionnaire. Ophthalmol Ther. 2021 Jun;10(2):299-311. doi: 10.1007/s40123-021-00335-4. Epub 2021 Feb 23.
Results Reference
derived

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Omega 3 and Vitamin D Dosage in a Population With Moderate to High Risk of AMD

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