NCT07892911

Brief Summary

This is a randomized, triple-blind, placebo-controlled clinical trial evaluating the effects of the Ancestral Supplements Grass Fed Beef Liver oral supplement on energy, mood, and mental clarity over 12 weeks. One hundred male and female participants aged 18-50 who report concerns regarding energy levels, mood, and mental clarity will be enrolled and randomized equally into an intervention arm (beef liver supplement) or a placebo arm. Participants will take their assigned product once daily and complete self-reported questionnaires at Baseline, Week 4, Week 8, and Week 12. Blood testing (iron panel) will be conducted at Baseline and Week 12 at a local Quest Diagnostics Clinic. The primary objective is to evaluate the product's effects on energy and mood; the secondary objective is to assess participants' perceptions of the product's effects on energy, mood, and mental clarity, including happiness, anxiety, well-being, brain fog, and concentration.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
1mo left

Started Sep 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress58%
Sep 2026Dec 2026

Study Start

First participant enrolled

September 1, 2026

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

October 19, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

October 23, 2026

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

October 23, 2026

Status Verified

October 1, 2026

Enrollment Period

3 months

First QC Date

October 19, 2026

Last Update Submit

October 19, 2026

Conditions

Outcome Measures

Primary Outcomes (3)

  • Change in Iron Status

    Change in blood iron levels assessed via iron panel blood test (Quest Diagnostics, iron test code 001339)

    Baseline and Week 12

  • Change in Energy Levels

    Change in self-reported energy levels assessed via self-reported questionnaire

    Baseline, Week 4, Week 8, and Week 12

  • Change in Mood

    Change in self-reported mood assessed via self-reported questionnaire

    Baseline, Week 4, Week 8, and Week 12

Secondary Outcomes (6)

  • Change in Self-Reported Vitality

    Baseline, Week 4, Week 8, and Week 12

  • Change in Self-Reported Happiness

    Baseline, Week 4, Week 8, and Week 12

  • Change in Self-Reported Anxiety

    Baseline, Week 4, Week 8, and Week 12

  • Change in Self-Reported Well-being

    Baseline, Week 4, Week 8, and Week 12

  • Change in Self-Reported Brain Fog

    Baseline, Week 4, Week 8, and Week 12

  • +1 more secondary outcomes

Study Arms (2)

Intervention (Beef Liver Supplement)

EXPERIMENTAL
Dietary Supplement: Intervention

Placebo Comparator

PLACEBO COMPARATOR
Dietary Supplement: Placebo

Interventions

InterventionDIETARY_SUPPLEMENT

Participants receive the Ancestral Supplements Grass Fed Beef Liver supplement (Grass Fed Liver \[Bovine\], 3000 mg per serving of 6 capsules) taken once daily, with a graduated dose escalation from 1 capsule/day over the first 18 days up to the full serving of 6 capsules/day, for 12 weeks.

Intervention (Beef Liver Supplement)
PlaceboDIETARY_SUPPLEMENT

Participants receive a matched placebo product (microcrystalline cellulose and natural food color) taken once daily using the same dosing regimen as the intervention arm, for 12 weeks. The taste and appearance of the placebo are matched to the test product.

Placebo Comparator

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Be male or female
  • Be aged 18-50
  • Anyone experiencing issues regarding all of the following over the past four weeks: energy levels, mood, and mental clarity
  • Anyone who is generally healthy - does not live with any uncontrolled chronic disease
  • Anyone who is willing to maintain their current diet, sleep schedule, and activity level for the duration of the study
  • Resides in the United States

You may not qualify if:

  • Anyone with pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders
  • Currently taking iron supplements or being treated for anemia
  • Anyone currently taking oral contraceptives that contain iron
  • Anyone currently taking vitamin A supplements, or supplements that contain vitamin A
  • Anyone with any allergies or sensitivities to any of the study product ingredients
  • Any women who are pregnant, breastfeeding, or trying to conceive (or who will be at any point during the study period)
  • Anyone with hemochromatosis
  • Anyone unwilling to follow the study protocol
  • Has stopped using hormonal birth control in the past month
  • Anyone who is vegan and/or does not consume animal products for any reason
  • Anyone who is considered to be a heavy drinker (i.e. 8 or more alcoholic drinks per week for women or 15 or more alcoholic drinks per week for men)
  • Planning on introducing any products or any new forms of prescription medication or supplements that target energy levels, mood, or mental clarity, during the study duration
  • Currently partaking in another research study or will be partaking in any other research study at any point during this study's duration

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Citruslabs

Las Vegas, Nevada, 89118, United States

Location

MeSH Terms

Conditions

FatigueConsciousness DisordersIron DeficienciesMental Fatigue

Interventions

Methods

Condition Hierarchy (Ancestors)

Signs and SymptomsPathological Conditions, Signs and SymptomsNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesNeurocognitive DisordersMental DisordersIron Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesBehavioral SymptomsBehavior

Intervention Hierarchy (Ancestors)

Investigative Techniques

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 19, 2026

First Posted

October 23, 2026

Study Start

September 1, 2026

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 1, 2026

Last Updated

October 23, 2026

Record last verified: 2026-10

Locations