Intervention Trial in Early Age-related Macular Degeneration (I-TEAM)
Primary Purpose
Age-related Macular Degeneration (AMD)
Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Lutein-enriched-egg beverage (NWT-02)
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Age-related Macular Degeneration (AMD) focused on measuring AMD, Lutein, Visual function, Early signs of AMD, AREDS-category 2
Eligibility Criteria
Inclusion Criteria:
Early AMD (AREDS category 2)
- many small drusen, or
- a few intermediate-sized (63-124 micrometres in diameter) drusen, or
- macular pigmentary changes
OR
Intermediate AMD (AREDS category 3)
- extensive intermediate sized (63-124 micrometres in diameter) drusen, or
- at least one large (>125 micrometers in diameter) drusen or
- geographic atrophy not involving the foveal centre
- men and women age ≥50 years
- BMI 18-35 kg/m2
- Vision ≥ 20/40 for Snellen visual acuity
- lutein intake of < 2 mg/day (including supplements)
- DHA intake of < 150 mg/day (including supplements)
- must be able to give written informed consent
- have normal hematologic parameters
- normal values of plasma albumin
- normal values for liver and kidney function
- no use of carotenoid, fish oil, or n3 fatty acid supplements (within 1 month of study start)
Exclusion Criteria:
- ocular media opacity (severe cataract)
- history of active small bowel disease or resection
- atrophic gastritis
- history of hyperlipidemia or screening values as follows (LDL > 5.33mmol/L or 205mg/dL; triglycerides > 4.52mmol/L or >400 mg/dL)
- hypertension (>150/90 mm Hg)
- diabetes mellitus (if also accompanied by signs of diabetic retinopathy)
- alcohol intake of >2 drinks/day or 14 drinks/week
- pancreatic disease
- dementia or Alzheimer's disease
- anemia, and bleeding disorders
- known allergy to egg or egg products
- known allergy to milk or milk products
- known allergy to cocoa or chocolate products
- known allergy to fish or fish oils
- lactose intolerance
- pregnancy or lactation
- diseases that interfere with fat absorption, e.g. colitis, celiac disease, Crohn's disease, cystic fibrosis (as determined by screening interview)
- medication or supplements that contain a significant level of carotenoids, including an amount of lutein of more than 0.25 mg per day within 1 month of the study start
- medications that interfere with fat absorption, e.g. bile sequestrants (as determined by screening interview)
- use of antipsychotic, anti manic, or dementia medications
- smoking or use of nicotine patches or gum (within the past 6 months)
- subjects having extremely high dietary intakes of carotenoids
- stroke, head injury with loss of consciousness or seizures
- for US and UK center: Non English speaking
Sites / Locations
- TUFTS University
- Universitäts Augenklinik - Bonn
- Radboud University Hospital
- Manchester Royal Eye Hospital - Manchester
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Lutein-enriched-egg beverage
Placebo
Arm Description
Powder in sachets is provided and dissolved to prepare Lutein-enriched-egg beverage
Powder in sachet to prepare beverage
Outcomes
Primary Outcome Measures
Visual function
Secondary Outcome Measures
Carotenoid levels
Levels of lutein and Zeaxanthin
Full Information
NCT ID
NCT01694680
First Posted
September 25, 2012
Last Updated
September 20, 2016
Sponsor
Newtricious R&D BV
Collaborators
Sprim Advanced Life Sciences
1. Study Identification
Unique Protocol Identification Number
NCT01694680
Brief Title
Intervention Trial in Early Age-related Macular Degeneration
Acronym
I-TEAM
Official Title
Intervention Study to Assess the Effect of Daily Consumption of a Lutein-enriched-egg Beverage on Maintenance of Visual Function in Subjects With Early Signs of Age-related Macular Degeneration
Study Type
Interventional
2. Study Status
Record Verification Date
September 2016
Overall Recruitment Status
Completed
Study Start Date
October 2012 (undefined)
Primary Completion Date
April 2016 (Actual)
Study Completion Date
April 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Newtricious R&D BV
Collaborators
Sprim Advanced Life Sciences
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of the I-TEAM project is to assess whether there is a change in visual function and status of the retina after a year of intervention in subjects with early signs of Age-related Macular Degeneration.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Age-related Macular Degeneration (AMD)
Keywords
AMD, Lutein, Visual function, Early signs of AMD, AREDS-category 2
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
120 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Lutein-enriched-egg beverage
Arm Type
Active Comparator
Arm Description
Powder in sachets is provided and dissolved to prepare Lutein-enriched-egg beverage
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Powder in sachet to prepare beverage
Intervention Type
Dietary Supplement
Intervention Name(s)
Lutein-enriched-egg beverage (NWT-02)
Intervention Description
Lutein, zeaxanthin and DHA-enriched-egg yolk combined with buttermilk beverage
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
color-, taste- and energy-matched powder without enriched egg-yolk
Primary Outcome Measure Information:
Title
Visual function
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Carotenoid levels
Description
Levels of lutein and Zeaxanthin
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Early AMD (AREDS category 2)
many small drusen, or
a few intermediate-sized (63-124 micrometres in diameter) drusen, or
macular pigmentary changes
OR
Intermediate AMD (AREDS category 3)
extensive intermediate sized (63-124 micrometres in diameter) drusen, or
at least one large (>125 micrometers in diameter) drusen or
geographic atrophy not involving the foveal centre
men and women age ≥50 years
BMI 18-35 kg/m2
Vision ≥ 20/40 for Snellen visual acuity
lutein intake of < 2 mg/day (including supplements)
DHA intake of < 150 mg/day (including supplements)
must be able to give written informed consent
have normal hematologic parameters
normal values of plasma albumin
normal values for liver and kidney function
no use of carotenoid, fish oil, or n3 fatty acid supplements (within 1 month of study start)
Exclusion Criteria:
ocular media opacity (severe cataract)
history of active small bowel disease or resection
atrophic gastritis
history of hyperlipidemia or screening values as follows (LDL > 5.33mmol/L or 205mg/dL; triglycerides > 4.52mmol/L or >400 mg/dL)
hypertension (>150/90 mm Hg)
diabetes mellitus (if also accompanied by signs of diabetic retinopathy)
alcohol intake of >2 drinks/day or 14 drinks/week
pancreatic disease
dementia or Alzheimer's disease
anemia, and bleeding disorders
known allergy to egg or egg products
known allergy to milk or milk products
known allergy to cocoa or chocolate products
known allergy to fish or fish oils
lactose intolerance
pregnancy or lactation
diseases that interfere with fat absorption, e.g. colitis, celiac disease, Crohn's disease, cystic fibrosis (as determined by screening interview)
medication or supplements that contain a significant level of carotenoids, including an amount of lutein of more than 0.25 mg per day within 1 month of the study start
medications that interfere with fat absorption, e.g. bile sequestrants (as determined by screening interview)
use of antipsychotic, anti manic, or dementia medications
smoking or use of nicotine patches or gum (within the past 6 months)
subjects having extremely high dietary intakes of carotenoids
stroke, head injury with loss of consciousness or seizures
for US and UK center: Non English speaking
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
E J Johnson, PhD
Organizational Affiliation
Jean Mayer USDA Human Nutrition Research Center on Aging (HNRCA), Boston
Official's Role
Principal Investigator
Facility Information:
Facility Name
TUFTS University
City
Boston
State/Province
Massachusetts
Country
United States
Facility Name
Universitäts Augenklinik - Bonn
City
Bonn
Country
Germany
Facility Name
Radboud University Hospital
City
Nijmegen
ZIP/Postal Code
6525EX
Country
Netherlands
Facility Name
Manchester Royal Eye Hospital - Manchester
City
Manchester
Country
United Kingdom
12. IPD Sharing Statement
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Intervention Trial in Early Age-related Macular Degeneration
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