MIRIA fractional laser treatment for changes in metabolism, weight, and body composition

You may qualify if

• 18- 60 years of age;
• BMI between 25.0 and 30 kg/m2;
• Subjects must be in good general health, based on answers provided during the screening visit;
• Subject must be able and willing to provide written informed consent and comply with the requirements of the study protocol.
• Females of childbearing potential must be willing and able to use a medically highly effective form of birth control during the entire study.

You can't join if

• Participation in another investigational drug or device clinical trial in the past 30 days;
• Currently pregnant or pregnancy within the past 6 months or currently breastfeeding;
• Have a history of drug or alcohol abuse in the past 3 years or have reported habitual alcohol intake greater than 2 standard drinks per day (e.g., 2 beers, 2 glasses of wine, or 2 mixed drinks);
• Planning or currently participating in a weight loss program;
• Plan to change daily diet or level of physical activity;
• Intake of medication that may affect body weight such as GLP-1 receptor agonists, amitriptyline, bupropion, thyroid medications, etc.;
• History of cancer which required lymph node biopsy or dissection;
• Weight loss or gain of 10 kg or more in the past 6 months;
• History of diabetes mellitus or cardiac disease;
• Intake of hormone replacement therapy (HRT) in the last 6 months;
• Infection, surgery, or history of trauma or laser treatment to the treatment area in the past 6 months;
• Presence of any skin disease on the abdomen or thighs;
• Have birthmarks, tattoos, scars, or any other disfiguration of the skin in the abdomen or thighs;
• Presence of sunburn or tan in the abdomen or thighs;
• Use of any topical application of retinoids in the past 6 weeks on the abdomen or thighs or intake of systemic retinoids in the past 6 months;
• Use of any prescription topical medication, such as corticosteroids or hydroquinone on the abdomen or thighs in the past 6 weeks;
• History of keloid formation or hypertrophic scarring;
• History of bariatric surgery or other major weight-loss procedures;
• History of abdominal liposuction, abdominoplasty or CoolSculpting;
• Known allergy to lidocaine or other local anesthetics;
• The investigator believes that the subject is an unsuitable candidate to participate in the study, receive laser treatment, or would be placed at risk by participating in the study.