40 Participants Needed

Blue Burn Tincture for Fatigue

No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

Trial Summary

What is the purpose of this trial?

This study will evaluate the effects of the Blue Burn Tincture on energy levels, weight management, and markers of metabolic health. It is a single-arm, hybrid trial involving 40 participants over a 12-week period. Participants will use the product daily, complete scheduled questionnaires, attend blood tests at Labcorp (Baseline and Week 12), and provide body mass measurements. Primary outcomes include changes in cortisol levels, energy levels, and body mass.

Eligibility Criteria

This trial is for individuals experiencing fatigue and stress who are interested in managing their weight and improving metabolic health. Participants must be willing to use the Blue Burn Tincture daily, answer questionnaires, go for blood tests at Labcorp twice, and measure their body mass regularly over a 12-week period.

Inclusion Criteria

Own a body weight scale
Exercise at least once per week
Willing to maintain study protocol and refrain from certain products/supplements during study duration
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Exclusion Criteria

Pre-existing chronic conditions that would prevent adherence to protocol, including oncological and psychiatric disorders
Had a major illness in the last three months
Heavy alcohol consumption
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Timeline

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive 4 mL of the Blue Burn Tincture daily for 12 weeks, complete questionnaires, and attend blood tests at Baseline and Week 12

12 weeks
2 visits (in-person) at Baseline and Week 12

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

Treatment Details

Interventions

  • Blue Burn Tincture
Trial Overview The study is testing the Blue Burn Tincture's ability to boost energy levels, aid in weight management, and improve markers of metabolic health like cortisol levels. It's a single-arm trial with all participants using the tincture without comparison to a placebo or other treatment.
Participant Groups
1Treatment groups
Experimental Treatment
Group I: Blue Burn Tincture GroupExperimental Treatment1 Intervention
Participants will receive 4 mL of the Blue Burn Tincture daily for 12 weeks. The dose is split into 2 mL in the morning and 2 mL at lunchtime (before 2 PM), mixed with water or another liquid.

Find a Clinic Near You

Who Is Running the Clinical Trial?

Apothekary

Lead Sponsor

Trials
1
Recruited
80+

Citruslabs

Industry Sponsor

Trials
94
Recruited
5,100+
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