MGH Clinical Unit for Research Trials & Outcomes in Skin
Boston, Massachusetts, 02114, United States
NCT Number: NCT06899958
This is a single-center, open-label pilot study to determine the effect of large area fractional laser treatment (LAFLT) on adults' metabolic profile.
Trial opening soon.
Get Notified18 year–60 year
All sexes
Interventional
Not applicable
Boston, Massachusetts, 02114, United States
The current research project aims to investigate the effects of large-area fractional laser treatment (LAFLT) on body weight, metabolism, and body composition. Prior research suggests that treating large skin areas with fractional laser therapy may stimulate metabolism and promote weight loss. The MIRIA laser, an FDA-approved fractional laser, is widely used for skin aging, acne scarring, and wrinkle reduction and will be used to evaluate these potential metabolic effects.
Subjects aged 18-60 with a BMI of 25-30 will undergo three fractional laser treatments on the abdomen and thighs over 36 weeks, with sessions every four weeks. The study includes six total visits, incorporating photography, non-invasive imaging, x-rays, blood draws, and two optional biopsies.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Three fractional laser treatments to the abdomen and thighs at 4 week intervals.
Time frame: Week 1, 12, 24
The percent body fat will be collected from the Dual energy x-ray absorptiometry scan (DEXA) and via the Bioelectrical Impedance Analysis (BIA).
Time frame: Week 0, 4, 8, 12, 24
BMI will be calculated using the formula: weight (kg) / [height (m)]². Height will be measured at the baseline visit and body weight will be measured at each of the following visits.
Time frame: Week 0, 4, 8, 12, 24
These measurements will be taken at each of the following visits
Time frame: Week 0, 4, 8, 12, 24
These measurements will be taken at each of the following visits
Time frame: Week 0, 4, 8, 12, 24
These measurements will be taken at each of the following visits
Time frame: Week 1, 12, 24
The total lean body mass will be collected from the Dual energy x-ray absorptiometry scan (DEXA) and via the Bioelectrical Impedance Analysis (BIA).
Time frame: Week 0, 4, 8, 12, 24
Measurement of red blood cell count, white blood cell count, hemoglobin, hematocrit, and platelet count via a blood draw.
Time frame: Week 0, 4, 8, 12, 24
Assessment of glucose, calcium, electrolyte and fluid balance (sodium, potassium, CO2, chloride), kidney function (BUN, creatinine), and liver function (albumin, total protein, ALP, ALT, AST, bilirubin) via a blood draw.
Time frame: Week 0, 4, 8, 12, 24
Measurement of total cholesterol, HDL cholesterol, LDL cholesterol, and triglycerides via a blood draw.
Time frame: Week 0, 4, 8, 12, 24
Measurement of hemoglobin A1c via a blood draw.
Time frame: Week 0, 4, 8, 12, 24
Measurement of CRP levels via a blood draw.
Time frame: Week 0, 4, 8, 12, 24
Assessment of the rate at which red blood cells sediment via a blood draw.
Time frame: Week 0, 4, 8, 12, 24
Measurement of plasma histamine levels via a blood draw.
Time frame: Week 0, 4, 8, 12, 24
Measurement of serum cortisol levels via a blood draw.
Time frame: Week 0, 4, 8, 12, 24
Measurement of serum oxytocin levels via a blood draw.
Time frame: Week 0, 4, 8, 12, 24
Measurement of serum CPK via a blood draw.
Time frame: Week 0, 4, 8, 12, 24
Measurement of interleukin-6 (IL-6) via a blood draw.
Time frame: Week 0, 4, 8, 12, 24
Measurement of norepinephrine via a blood draw.
Time frame: Week 0,12, 24
This is a non-invasive procedure that measures how much energy the body uses.
Time frame: Week 1, 12
2 optional biopsies will be take pre- and post-laser treatment to measure changes in collagen and skin thickness.
Time frame: Week 0, 4, 8, 12, 24
Ultrasound will be used to measure skin elasticity.
Time frame: Week 0, 4, 8, 12, 24
Ultrasound will be used to measure skin thickness.
Time frame: Week 0, 12
Estimation of total body water content as a percentage of body weight using the Bioelectrical impedance analysis (BIA).
Time frame: Week 1, 4, 8
The visual analog scale (VAS) pain score will be collected from the subject after each laser treatment. The VAS is a 10cm long scale with 0cm representing "no pain" and 10cm representing "worst possible pain".
Time frame: Week 1, 12, 24
The total body BMD will be collected from the Dual energy x-ray absorptiometry scan (DEXA).
Contact information is provided by the study sponsor or research team.
Alicia Van Cott, NP
CONTACT
Maria Alora, MD
CONTACT
Massachusetts General Hospital
Other
Acronym: MELT
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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