Efficacy of a Dietary Supplement Powder Formula (Daily Ultimate Essentials) in an Adult Population.

Prenetics Global

Status and phase

Active, not recruiting

Phase 4

Conditions

Dietary Assessment

Treatments

Dietary Supplement: REDS Powder

Study type

Interventional

Funder types

Industry

Identifiers

NCT06655597

PR20240501

Details and patient eligibility

About

Healthy Adult subjects

Full description

The study will be a prospective randomized, controlled clinical study. There will be interventional treatment for a total of 12 weeks. The subjects will attend two appointments in the clinic throughout the duration of the study.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

BMI between 18.5 and 30 kg/m2
Low, moderate, and high activity (self-identified) *
Self-identify as having fatigue, and abdominal issues (bloating, constipation etc.) *
Participants will be able to read, understand and sign an informed consent form (includes HIPAA and States requirements) and sign a photo release form.
Participants are willing and able to follow all study directions, attend study visits as scheduled and must be willing to accept the restrictions of the study including but not limited to:
Willing to refrain from introducing any new diets or dietary supplements for the duration of the study

Exclusion criteria