Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
University of Minnesota
Age
30–65
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Subjects who are able to give voluntary, written informed consent to participate in this study and from whom consent has been obtained including HIPPA Authorization
Healthy men and women, ages 30 - 65 years of age
Subjects with Fitzpatrick photo skin type I-VI
Subjects with moderate to severe nasolabial folds contour deficiencies or other facial wrinkles. Degree of nasolabial folds or other facial wrinkles will be determined on the basis of the Wrinkles Severity Rating Scale
Subjects who agree not to have any other procedures of affecting skin quality (microdermabrasion, peels, acne treatments, toxin, fillers etc.) for the duration of the study
Subjects who understand the study and are able to follow study instructions and are willing to attend the required study visits.
Subjects who agree to be photographed for research purposes and their identity may not be concealed in these photographs.
You may not be if
Subjects who have had any kind of aesthetic therapy (peeling, laser, ultrasound, toxins, fillers) in the facial area during the last 6 months
Presence of implant in the facial area to treat
Contraindications to the use of antiseptics (Biseptine, Amukine)
Subjects who have an active or known skin inflammation or infection within the treatment area.
Subjects who have an active or known acute skin allergies
Subjects who have a known allergy to hyaluronic acid
Subjects who have any other dermatologic conditions including acne, rosacea, eczema, psoriasis, actinic keratosis, severe sun damage, infection, or scars within the treatment area.
Subjects of child-bearing potential who are not using an approved method of birth control (oral contraceptives, IUD, contraceptive implant, barrier methods with spermicide or abstinence). Females of non-childbearing potential are defined as post-menopausal (absence of menstrual bleeding for one year), hysterectomy, or bilateral oophorectomy.
Subjects who are pregnant, planning to become pregnant or breastfeeding. A urine pregnancy test will be done to rule out pregnancy.
Subjects who have been diagnosed with diabetes
Subjects who are Immunosuppressed
Subjects who are HIV+ / VHB+ / VHC+
Subjects who have had/will have a COVID vaccine within 2 weeks of study participation
Subjects who have had/will have a dental procedure within 4 weeks of study participation
