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New treatment option for Autophagy
Official title Effects of Miricell Supplementation on Biomarkers of Healthy Aging and Autophagy
ClinicalTrials.gov ID: NCT07675200
What this study is testing
- What it's testing
- The goal of this clinical trial is to learn if a dietary supplement called Miricell works to improve cellular health and signs of healthy aging in adults. It will also learn about the safety of Miricell.
- You might receive a placebo (an inactive treatment) instead of the study drug, decided by chance. You may not know which one you got.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 40 to 70. Healthy volunteers may be eligible.
You may be able to join if
- Provide voluntary signed and dated informed consent.
- Be in fair health as determined by medical history and routine blood chemistries.
- Age between the ages of 40 and 70 (inclusive).
- Body weight of at least 110 pounds.
- Normotensive (seated, resting systolic blood pressure \<140 mm Hg and diastolic blood pressure \< 90 mm Hg. If the first measurement is slightly...
You likely can't join if
- Use of probiotics, postbiotics or antibiotics within the past month.
- A history of unstable or new-onset cardiovascular/cardiorespiratory, liver, or renal disease.
- The participant's alcohol consumption is more than two standard alcoholic drinks per day or more than 10 drinks per week or has a history of...
- History of diabetes (any form) or any endocrine disorder.
- Fasting blood sugar of \> 125 mg/dL.
- Current smokers who smoke 11 or more cigarettes per day (i.e. light smokers will be enrolled if they meet all other criteria).
See the full eligibility criteria
- Provide voluntary signed and dated informed consent.
- Be in fair health as determined by medical history and routine blood chemistries.
- Age between the ages of 40 and 70 (inclusive).
- Body weight of at least 110 pounds.
- Normotensive (seated, resting systolic blood pressure \<140 mm Hg and diastolic blood pressure \< 90 mm Hg. If the first measurement is slightly elevated above these limits, the subject will be given a brief (5-minute)...
- Normal seated, resting heart rate (\<90 per minute).
- Willing to duplicate their previous 24-hour diet, refrain from alcohol for 24 hours, exercise for 24 hours prior to each trial, caffeine for 12 hours prior to each trial, and fast for 10 hours prior to each of the...
- Participant agrees to maintain existing dietary and physical activity patterns throughout the study period.
- Participant is willing and able to comply with the study protocol.
- If a dietary supplement was initiated within the past month, the participant is willing to discontinue supplement use followed by a 2-week washout prior to participation in the study.
- Able to provide an adequate blood draw.
- Use of probiotics, postbiotics or antibiotics within the past month.
- A history of unstable or new-onset cardiovascular/cardiorespiratory, liver, or renal disease.
- The participant's alcohol consumption is more than two standard alcoholic drinks per day or more than 10 drinks per week or has a history of drug/alcohol abuse or dependence.
- History of diabetes (any form) or any endocrine disorder.
- Fasting blood sugar of \> 125 mg/dL.
- Current smokers who smoke 11 or more cigarettes per day (i.e. light smokers will be enrolled if they meet all other criteria).
- History of hyperparathyroidism or an untreated thyroid disease.
- History of malignancy in the previous five years except for non-melanoma skin cancer (basal cell cancer or squamous cell cancer of the skin).
- Chronic inflammatory condition or disease (e.g., rheumatoid arthritis, Crohn's Disease, ulcerative colitis, lupus, HIV/AIDS, etc.).
- Previous medical diagnosis of gout or fibromyalgia.
- Any female who is pregnant, trying to become pregnant, is less than/or equal to 120 days postpartum, or any current women who are nursing.
- Women who participate in this study must agree to the use of contraception for the duration of the study, and any sexually active woman will have to take a negative pregnancy test prior to enrolling. Women of...
- Known allergy or sensitivity to any ingredient in the test formulations as listed on the product label.
- Any other diseases or conditions that, in the opinion of the medical staff, could confound the primary endpoints or place the subject at increased risk of harm if they were to participate.
The study team makes the final eligibility decision.
Where it's taking place
- Canfield, Ohio, United States
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 40 years to 70 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Canfield, Ohio, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.