Novel Laboratory Methods in Nutrition Studies

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