Is NCT07675200 recruiting in Canfield, OH?

Yes, NCT07675200 is currently recruiting participants at its Canfield, OH location. This autophagy clinical trial is actively enrolling qualified participants.

How do I join the autophagy clinical trial in Canfield?

To join this clinical trial in Canfield, complete the eligibility form on this page. A study coordinator will contact you to discuss next steps and determine if you qualify.

Is participation in this Canfield clinical trial free?

Yes, all study-related care is provided at no cost to qualified participants. Many studies also offer compensation for time and travel expenses.

Autophagy Clinical Trial in Canfield, OH

About This Autophagy Study in Canfield

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. The main questions it aims to answer are: * Does Miricell improve markers of autophagy, which is the body's natural process for recycling damaged cells? * Does Miricell support brain health, metabolic health, and visible signs of aging? * What medical problems, if any, do participants experience while taking Miricell? Researchers will compare Miricell to a placebo (a look-alike capsule that contains no active ingredients) to see if Miricell works better to support healthy aging. Participants will: * Take either one Miricell capsule or a placebo every day for 12 weeks with a morning meal. * Visit the research clinic four times over the course of the study for checkups and tests. * Complete memory and thinking tests, track their daily physical activity, and give blood samples to measure health changes.

Sponsor: Nutraland USA, Inc.

Who Can Participate

Inclusion 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) rest period, and two more measurements will be taken. The average of all three measurements will be used to determine eligibility.

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 treatments.

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.

Exclusion Criteria

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 childbearing age (any woman prior to menopause), regardless of their use of contraception, will be provided a urine pregnancy test kit at their screening visit and take the test in private using the female lavatory after signing an informed consent.

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.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Canfield?

Yes, this clinical trial (NCT07675200) has an active research site in Canfield, OH that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Autophagy Treatment Options in Canfield, OH

If you're searching for autophagy treatment options in Canfield, OH, this clinical trial (NCT07675200) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Canfield research site is actively enrolling participants for this clinical trial. You'll receive care from experienced autophagy specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all autophagy clinical trials near you to find additional studies recruiting in your area.

Autophagy Clinical Trial in Canfield, OH

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