Phase
Condition
Respiratory Syncytial Virus (Rsv) Infection
Treatment
Mitoquinone mesylate (MitoQ)
Placebo
Cold Air Exposure
Clinical Study ID
Ages 18-40 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Male or female, age 18-40
In good health as determined by OMSO (Office of Medical Support and Oversight)
Willing to refrain from exercise and caffeinated or alcoholic beverages for 12 hoursbefore each testing session
Willing to refrain from antioxidant-rich foods, such as blueberries, pecans, anddark chocolate, 48 h before each testing session
Eumenorrheic females (menstrual cycle length between 24-35 days) or females takingoral contraceptives, or utilizing implantable contraception (e.g., intrauterinedevice)
Have supervisor approval if active-duty military or a federal employee at NSSC
Exclusion
Exclusion Criteria:
History of cold injuries of any severity (e.g., frostbite, trench foot, chilblains)
Raynaud's syndrome
Cold-induced asthma/bronchospasm
Previous hand/finger injuries that impair dexterity and hand function
Metal hardware (plates/screws) in the forearms and hands
Smoke, vape, or use smokeless tobacco or other nicotine-containing productshabitually (unless have quit > 4 months prior)
Current use of medications (except for birth control) or dietary supplements thatcould alter cardiovascular, thermoregulatory, or vascular control (e.g.,anti-hypertensives, statins)
History of disease of the gastrointestinal tract including (but not limited to)diverticulosis, diverticulitis and inflammatory bowel disease, peptic ulcer disease,Crohn's disease, ulcerative colitis; or previous gastrointestinal surgery
Have a history of renal disease including (but not limited to) chronic kidneydisease, acute kidney injury, kidney stone disease, glomerular disease, or nephritis
Known allergies to medical adhesives
Known allergy to MitoQ
Difficulty swallowing pills
Heart, lung, kidney, muscle, or nerve disorder(s)
A planned MRI during the study or within 3 days after completing a cold test
Women who are pregnant, planning to become pregnant, or breastfeeding
Not willing to have small areas of skin on the body shaved (if deemed necessary forattachment of study instrumentation)
Have donated blood within 8 weeks of the study or plan to donate blood during thestudy
Lesions on a significant portion of the upper extremities due to skin pigmentationdisorders (e.g., vitiligo, psoriasis)
Study Design
Study Description
Connect with a study center
U.S. Army Research Institute of Environmental Medicine
Natick, Massachusetts 01760
United StatesActive - Recruiting
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