Study of the Effectiveness of Green Diode Laser Light on Body Shaping

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Erchonia Corporation
ClinicalTrials.gov Identifier:
NCT01292538
First received: February 8, 2011
Last updated: May 7, 2014
Last verified: May 2014
  Purpose

The purpose of this study is to determine if 532nm green diode laser light is effective in body contouring of the waist, hips and thighs.


Condition Intervention
Body Contouring
Device: Erchonia GLS
Device: Placebo laser

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: A Double-blind, Placebo-controlled Randomized Evaluation of the Effect of the Erchonia Scanner Device (GLS) Green Diode on Body Contouring of the Waist, Hips and Thighs

Further study details as provided by Erchonia Corporation:

Primary Outcome Measures:
  • Combined Circumference in Inches of the Waist, Hips and Bilateral Thighs [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]
    Mean change in total combined circumference inches of the waist, hips and bilateral thighs from baseline to endpoint evaluation.


Secondary Outcome Measures:
  • Body Mass Index (BMI) [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]
  • Subject Self-reported Satisfaction With Study Outcome [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]
  • Body Weight (Pounds) [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]

Enrollment: 67
Study Start Date: February 2011
Study Completion Date: June 2012
Primary Completion Date: June 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Erchonia GLS 532nm
532nm green laser light therapy.
Device: Erchonia GLS
532 nm green diode low level laser light device
Sham Comparator: Placebo laser
Sham light output with no therapeutic benefit
Device: Placebo laser
Sham light output with no therapeutic benefit

Detailed Description:

Weight loss and body contouring are large, constantly-growing fields of cosmetic surgery. However, while the demand for body shaping procedures is constantly on the rise, so is the demand for such procedures to be performed more quickly, simply and most importantly, less invasively; hence the growing popularity of non- to minimally-invasive cosmetic surgery procedures. In 2005, more than 7.5 million minimally-invasive cosmetic procedures were performed, a 35% increase from 2000.

In recent years, Erchonia Corporation, a manufacturer of low level lasers, has developed a dual-diode laser that emits 532 nm and 635nm collimated line-generated beams to emulsify fat. In August, 2010, the Erchonia® ML Scanner (MLS) 635nm was cleared by FDA for use as a non-invasive dermatological aesthetic treatment for the reduction of circumference of hips, waist, and thighs. It was determined that the biochemical effect of the Erchonia® MLS stimulates the mitochondria of the adipocyte cells which in turn increases the production of ATP. The newly synthesized ATP triggers the up-regulation of cyclic adenosine monophosphate (cAMP). cAMP has been shown to stimulate cytoplasmic lipase, triggering the conversion of triglycerides into fatty acids and glycerol that can easily pass through the cell membrane. The transitory pore is evidence that the laser is allowing for the movement of fatty acids, glycerol, and triglycerides to pass across the membrane and into extra-cellular space. Through vasodilation of nearby blood vessels and arteries, oxidization of the triglycerides and fatty acids occurs within the extra-cellular space.

This pilot study will apply the Erchonia® MLS employing 532 nm green diodes in lieu of 635 nm red diodes to compare the results to those attained using the 635 nm diodes. The Sponsor believes the use of 532 nm diodes may prove as effective as 635 nm diodes combined with a reduction in total procedure administration time from 40 to 30 minutes. It is the goal of this study to evaluate this hypothesis.

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Body Mass Index (BMI) less than 30 kg/m²
  • Subject indicated for liposuction or use of liposuction techniques for the removal of localized deposits of adipose tissues that do not respond to diet and exercise; specifically for the indication of body contouring in the areas of the waist, hips and bilateral thighs. (As per the American Academy of Cosmetic Surgery's 2006 Guidelines for Liposuction Surgery).
  • Subject is willing and able to abstain from partaking in any treatment other than the study procedure to promote body contouring and/or weight loss during study participation.
  • Subject is willing and able to maintain his or her regular diet and exercise regimen without effecting significant change in either direction during study participation.

Exclusion Criteria:

  • Body Mass Index (BMI) of 30 kg/m² or greater.
  • Diabetic dependent on insulin or oral hypoglycemic medications.
  • Known cardiovascular disease.
  • Prior cardiac surgery.
  • Prior surgical intervention for body sculpting/weight loss, such as liposuction, abdominoplasty, stomach stapling, lap band surgery.
  • Medical, physical, or other contraindications for body sculpting/weight loss.
  • Use of medication(s) known to affect weight levels and/or to cause bloating or swelling and for which abstinence during study participation is not safe or medically prudent.
  • Any medical condition known to affect weight levels and/or cause bloating or swelling.
  • Diagnosis of, and/or taking medication for, irritable bowel syndrome.
  • Active infection, wound or other external trauma to the areas to be treated with the laser.
  • Photosensitivity disorder.
  • Current cancer or receiving treatment for cancer.
  • Pregnant, breast feeding, or planning pregnancy prior to study end.
  • Serious mental health illness such as dementia or schizophrenia; psychiatric hospitalization in past two years.
  • Developmental disability or cognitive impairment that would preclude adequate comprehension of the informed consent form and/or ability to record study measurements.
  • Involvement in litigation and/or a worker's compensation claim and/or receiving disability benefits related to weight-related/body shape issues.
  • Participation in research in the past 30 days.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01292538

Locations
United States, Indiana
Surgeon's Inc.
Marion, Indiana, United States, 46952
United States, Michigan
Bloomfield Laser and Cosmetic Surgery Center
Bloomfield Hills, Michigan, United States, 48302
Sponsors and Collaborators
Erchonia Corporation
Investigators
Principal Investigator: Gregory C Roche, MD, FACS
Principal Investigator: Robert F Jackson, MD, FACS
  More Information

No publications provided

Responsible Party: Erchonia Corporation
ClinicalTrials.gov Identifier: NCT01292538     History of Changes
Other Study ID Numbers: EC-GREEN001
Study First Received: February 8, 2011
Results First Received: April 1, 2014
Last Updated: May 7, 2014
Health Authority: United States: Institutional Review Board

ClinicalTrials.gov processed this record on October 19, 2014