Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 7:15 PM
Ignite Modification Date:
2025-12-24 @ 7:15 PM
NCT ID:
NCT07212803
Eligibility Criteria:
Inclusion Criteria:
* Healthy male or female adults 18-40 years of age
* Female participants of child-bearing potential must have a negative pregnancy test at the baseline visit
* Participants must be willing to refrain from caffeine and alcohol use 72 hours prior to sessions on study days
* Participants must be willing and able to: (1.) Consume up to 1 liter of fluid within a 30-minute period per visit (2.) Swallow a single large capsule per visit
* Participants must be willing to fast 10 hours prior to sessions on study days (only water is allowed during the fasting and active study period)
* Participants must have active health insurance throughout the duration of the study
Exclusion Criteria:
* Have a corrected QT (QTc) interval greater than 450 milliseconds (ms) for males or greater than 470 milliseconds (ms) for females, determined during the baseline visit
* Presence of any known medical condition, confirmed through participant interview. Examples of these include but not limited to: Dyslipidemia, Thyroid disease, Diabetes, Recurrent headache, Any psychiatric condition or neurological disorder, History of alcohol or drug abuse, Past diagnosis or history of renal insufficiencies, Hepatic dysfunction, Electrolyte imbalances requiring hospitalization
* Presence of any known heart/cardiac diseases or conditions such as: Atrial Fibrillation, History of stroke or heart attack, Hypertension, Heart Failure, Vascular Disease, Family history/Active Long QT Syndrome, Coronary artery disease, Cardiomyopathy, Valvular heart disease, Ventricular arrhythmia, Congenital heart defect, Pericardial disease, Myocarditis
* Study physician recommendation for participant to not be enrolled.
* Are underweight (BMI\<18.5 kg/m2, CDC 2024), have poor eating habits resulting in poor weight control, or have any factors that will put the participant at risk from fasting.
* Have any contraindications to the use of moxifloxacin, including a past medical history of myasthenia gravis, QT prolongation, or hypersensitivities and allergic reactions to moxifloxacin or any other fluoroquinolone antibiotics
* Pre-existing risk to tendinitis and tendon rupture, peripheral neuropathy, or central nervous system side effects
* Concurrent use of ANY medication taken daily including herbal products or supplements (daily basis is defined as greater than 2 days per week)
* Self-reported allergy to taurine
* Self-reported allergy to nuts (peanuts, pecans, cashews, etc.)
* Self-reported allergic reaction to the adhesive pads (electrodes, continuous glucose monitors, etc.)
* Fear of needle puncture
* Smokers using cigarettes, vaporized nicotine, or marijuana products currently or within the past month
* Current usage of any nicotine or tobacco products including but not limited to intranasal, sublingual, oral, or transdermal dosage forms
* Currently pregnant or breastfeeding
* Have a positive pregnancy test during the baseline visit
* Are currently enrolled in any other clinical study or have participated in another study within the last 30 days
* Non-English speaking/reading individuals will be excluded due to the unavailability of medically qualified translators throughout all study procedures
* If the candidate does not sign the informed consent document
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
40 Years
Study:
NCT07212803
Study Brief:
Protocol Section:
NCT07212803