Study of the Effect of Low Level Laser Light Therapy on Reducing the Appearance of Cellulite in the Thighs and Buttocks.

Inclusion Criteria

• Areas for which cellulite appearance reduction is being sought are the bilateral thighs and buttocks
• Clinical cellulite gradation of Stage II or III on the Nurnberger-Muller scale for each treatment area
• PI or P2 on the American Society of Anesthesiologists (ASA) Physical Status Classification System
• Willing and able to abstain from partaking in any treatment other than the study procedure to promote cellulite appearance reduction/body contouring/weight loss during the study
• Willing and able to maintain regular diet and exercise regimen without effecting significant change in either direction during the study
• Willing and able to maintain regular medication schedule, as is medically feasible, during the study

Exclusion Criteria

• Clinical cellulite gradation of Stage 0 or I on the Nurnberger Muller Scale (NMS) for either one or both thighs/buttocks
• P3 or P4 or P5 or P6 on the ASA Physical Status Classification System
• Weight fluctuation greater than 10 pounds in the prior month
• Previous attempt(s) to reduce cellulite in the study treatment areas over the past 6 months
• Prior surgical intervention to the treatment areas, for any reason
• Medical, physical or other contraindications for cellulite reduction/body contouring/weight loss
• Current use of medication(s) known to affect weight levels and/or cause bloating or swelling and for which abstinence during the study is not safe or medically prudent
• Any medical condition known to affect weight levels, cause bloating or swelling
• Diagnosis of, and/or taking medication for, irritable bowel syndrome
• Active infection, wound or other external trauma to the study treatment areas
• Dermatitis or significant scarring in the study treatment areas
• Medical, physical, or other contraindications for, or known sensitivity to, light therapy
• Diabetes dependent on insulin or oral hypoglycemic medications
• Known cardiovascular disease
• Cardiac surgeries
• History of deep venous thrombosis, arterial disease of the legs
• Pregnant, breast feeding, or planning pregnancy prior to study end
• Serious mental health illness or psychiatric hospitalization in past 2 years
• Developmental disability or cognitive impairment that would impact study participation
• Involved in litigation/receiving disability benefits related to the parameters of the study
• Participation in research in the past 30 days