Coolsculpting With Cooltone Verses Coolsculpting Alone for the Banana Roll Area

Not Applicable

• Conditions: Improved Appearance of the Banana Roll Region
• Interventions: Device: CoolSculpting Elite combined with CoolTone Treatments; Device: CoolSculpting Elite

• Registration Number: NCT05359614
• Lead Sponsor: Goldman, Butterwick, Fitzpatrick and Groff

Brief Summary

to evaluate the benefit and efficacy of CoolSculpting Elite study treatments versus CoolSculpting Elite study treatments followed by a series CoolTone for underneath the buttocks (also known as the banana roll).

Detailed Description

Investigate safety and efficacy of CoolSculpting Elite treatments for underneath the buttocks (also known as the banana roll) versus sequential treatments of CoolSculpting Elite and CoolTone for the banana roll region.

Study Timeline

• Study Start: 2022-03-14
• Study First Submitted: 2022-03-18
• Status Verified: 2022-04
• Study First Submitted QC: 2022-04-28
• Last Update Submitted: 2022-04-28
• Study First Posted: 2022-05-04
• Last Update Posted: 2022-05-04
• Primary Completion: 2022-08-30
• Study Completion: 2022-09-30

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: Female
• Target Recruitment: 15

Inclusion Criteria

• Inclusion Criteria

  1. Female ≥ 22 years and ≤65 years of age.
  2. Subject has not had weight change exceeding 5% of body weight in the preceding month.
  3. Subject agrees to maintain body weight within 5% during the study by not making any changes in diet or exercise routine.
  4. Subject has a BMI ≤ 30 as determined at screening.
  5. Subject agrees to have photographs taken of the treatment area(s) during the scheduled time periods.
  6. Subject agrees to refrain from any new or change in gluteal muscle training exercises of the treatment area during the course of the study.
  7. Subject agrees to avoid sun tanning or spray tanning during the course of the study. Subject has read and signed the study written informed consent form

Exclusion Criteria

• Exclusion Criteria

  1. Male Subjects
  2. Subject has had a recent surgical procedure(s) in the area of intended treatment and muscle contractions may disrupt the healing process.
  3. A subject with any uncontrolled systemic disease. A potential subject in whom therapy for a systemic disease is not yet stabilized will not be considered for entry into the study.
  4. A subject with a significant history or current evidence of a medical, psychological or other disorder that, in the investigator's opinion, would preclude enrollment into the study.
  5. Subject has had an invasive fat reduction procedure (e.g., liposuction, mesotherapy) non-invasive fat reduction or skin tightening procedures , or cellulite treatment in the area of intended treatment
  6. Subjects who tanned or spray tanned in the treatment area within the past 4 weeks
  7. A subject with history of or the presence of any skin condition/disease in the treatment area that might interfere with the diagnosis or evaluation of study parameters (i.e., atopic dermatitis, eczema, psoriasis, seborrheic dermatitis) at the discretion of the investigator.
  8. Subject needs to administer or has a known history of subcutaneous injections into the area of intended treatment (e.g., heparin, insulin) within the past month
  9. Subject hashad an intrauterine contraceptive device inserted or removed within the past month.
  10. A subject with an active bacterial, fungal, or viral infection in the treatment area.
  11. Subject has a bleeding disorder
  12. Subject has a blood disorder such as cryoglobulinemia, cold agglutinin disease and paroxysmal cold hemoglobinuria.
  13. Known sensitivity to cold such as cold urticaria, Raynaud's disease, pernio or Chilblains. Or patients with any impaired sensation in treated area
  14. A subject with scarring or tattoos in the treatment area that might interfere with the diagnosis or study evaluations at the discretion of the investigator.
  15. Subject is taking or has taken diet pills or supplements within the past month.
  16. Subject has a metal implant or active implanted device such as a cardiac pacemaker, cochlear implant, intrathecal pump, hearing aids, defibrillator, or drug delivery system.
  17. Subject has pulmonary insufficiency.
  18. Subject has a cardiac disorder.
  19. Subject has a malignant tumor.
  20. Subject has been diagnosed with a seizure disorder such as epilepsy.
  21. Subject currently has a fever.
  22. Subject is diagnosed with Grave's disease.
  23. Subject is pregnant or intending to become pregnant during the study period (in the next 9 months).
  24. Subject is lactating or has been lactating in the past 6 months.
  25. Subject is unable or unwilling to comply with the study requirements.
  26. Subject is currently enrolled in a clinical study of any other investigational drug or device.
  27. Current participation or participation within 30 days prior to the start of this study in a drug or other investigational research study.
  28. Any other condition or laboratory value that would, in the professional opinion of the investigator, potentially affect the subject's response or the integrity of the data or would pose an unacceptable risk to the subject

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
GROUP A=CoolSculpting Elite and CoolTone	CoolSculpting Elite combined with CoolTone Treatments	Group A: Study subjects will have a total of 1 or 2 bilateral CoolSculpting Elite sessions to the banana roll area 6 weeks prior to four EMMS treatment sessions during the study.
GROUP B CoolSculpting Elite alone	CoolSculpting Elite	Group B: Study subjects will have a total of 1 or 2 bilateral CoolSculpting Elite sessions to the banana roll area.

Primary Outcome Measures

Name	Time	Method
appearance of the banana roll region based on Investigator Global Aesthetic Improvement Scales	baseline to 18-weeks	Investigator Global Aesthetic Improvement Scale Scores will be assigned where -3 = Very Much Worse, -2 = Much Worse -, -1 = Worse, 0 = No Chance, 1 = Improved, 2 = Much Improved, 3 = Very Much Improved
Improvement in Appearance of the Banana Roll Region Based on Clinical Photographs	18 Weeks	Investigator Global Aesthetic Improvement Scale Scores where -3 = Very Much Worse, -2 = Much Worse -, -1 = Worse, 0 = No Chance, 1 = Improved, 2 = Much Improved, 3 = Very Much Improved will be assigned by a blinded assessor based on photographs

Secondary Outcome Measures

Name	Time	Method
Patient Treatment Satisfaction Survey	baseline to 18-weeks	Subject rating of treatment satisfaction where - 3 = Completely Dissatisfied, -2 = Moderately Dissatisfied, -1 = Mildly Dissatisfied, 0 = Neither Satisfied nor Dissatisfied, 1 = Mildly Satisfied, 2 = Moderately Satisfied, 3 =Completely Satisfied
Subject Global Aesthetic Improvement Scale	baseline to 18-weeks	Subject rating of treatment results where where -3 = Very Much Worse, -2 = Much Worse -, -1 = Worse, 0 = No Chance, 1 = Improved, 2 = Much Improved, 3 = Very Much Improved

Trial Locations

Locations (1)

West Dermatology Research Center/Cosmetic Laser Dermatology; 🇺🇸 San Diego, California, United States