Novel Laboratory Methods in Nutrition Studies

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Abbott

Status

Completed

Conditions

Healthy

Treatments

Other: Nutrition Products

Study type

Interventional

Funder types

Industry

Identifiers

NCT02732158
BL27

Details and patient eligibility

About

This prospective, nonrandomized, feasibility study will compare laboratory measures at the beginning and end of the study period in adults consuming a nutritional study product.

Enrollment

55 patients

Sex

All

Ages

55 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Participant must agree to refrain from taking supplements other than study product.
  • Participant states willingness to follow protocol as described, including consumption of study product per protocol, performing finger stick/DBS on Day 60 and completing any forms needed throughout the study.

Exclusion criteria

  • Body Mass Index (BMI) > or equal to 35 kg/m2
  • Has planned elective surgery requiring 2 or more days of hospitalization during the entire study
  • Has stated active malignant disease
  • Has a known history of chronic renal parenchymal disease
  • Has a known history of severe liver disease/liver failure
  • Has any psychiatric disorders that would interfere with study product consumption or compliance with the study procedures
  • Known allergy or intolerance to any study product ingredient
  • Participation in another study that has not been approved as a concomitant study

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

55 participants in 1 patient group

Nutrition Products
Experimental group
Description:
Two servings per day of the sachet study product mixed with water; 1 carotenoid capsule per day
Treatment:
Other: Nutrition Products

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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