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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
Newtricious R&D BV
About
Eligibility
Locations
Arms
Outcomes
Full info

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

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

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

First Posted
September 25, 2012
Last Updated
September 20, 2016
Sponsor
Newtricious R&D BV
Collaborators
Sprim Advanced Life Sciences
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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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