Multi-Center Traditional Feasibility Study of Radiofrequency Device

• Sponsor: Cynosure, Inc. (Industry)
• Overall Status: Recruiting
• CT.gov ID: NCT04584099
• Collaborator: (none)
• Enrollment: 20
• Locations: 2
• Arms: 4
• Anticipated Duration (Months): 28
• Patients Per Site: 10
• Patients Per Site Per Month: 0.4

Study Details

Study Description

Brief Summary

This is a prospective, controlled, multi-center study. Patients will be enrolled and treated with a radiofrequency device in this study if they have unwanted fat in the abdominal area.

Condition or Disease	Intervention/Treatment	Phase
Body Fat	Device: Radiofrequency device treatment	N/A

Detailed Description

Subjects are to be enrolled in this clinical study if they are 18 - 55 years old and are willing to have biopsies taken from a control site and the treatment area. Subjects may be enrolled if they have been previously scheduled or willing to have an abdominoplasty procedure after their participation in the study. A maximum of 20 subjects will be enrolled at up to 4 study centers. Subjects will attend a screening/pretreatment visit which may be performed on the same day as the treatment visit. Subjects may receive up to 5 treatments with the TempSure® Firm on the abdomen or flanks. All subjects will receive a phone call 1 week (1-10 days) post each treatment. Subjects may be asked to return for follow-up visits after their final treatment for incisional biopsies. A follow up may occur at 10, 20, and/or 30 days post their last treatment.

Study Design

• Study Type: Interventional
• Anticipated Enrollment: 20 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: None (Open Label)
• Primary Purpose: Basic Science
• Official Title: Histological Study to Assess Safety and Efficacy of the TempSure Firm for Non-invasive Lipolysis
• Actual Study Start Date: Aug 25, 2020
• Anticipated Primary Completion Date: Sep 25, 2022
• Anticipated Study Completion Date: Dec 25, 2022

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Immediately Post Treatment One radiofrequency treatment before scheduled biopsy or abdominoplasty on tissue to be removed during abdominoplasty immediately post treatment.	Device: Radiofrequency device treatment; TempSure firm
Experimental: 10 Days Post Treatment One radiofrequency treatment before scheduled biopsy or abdominoplasty on tissue to be removed during abdominoplasty 10 days post treatment.	Device: Radiofrequency device treatment; TempSure firm
Experimental: 20 Days Post Treatment One radiofrequency treatment before scheduled biopsy or abdominoplasty on tissue to be removed during abdominoplasty 20 days post treatment.	Device: Radiofrequency device treatment; TempSure firm
Experimental: 30 Days Post Treatment One radiofrequency treatment before scheduled biopsy or abdominoplasty on tissue to be removed during abdominoplasty 30 days post treatment.	Device: Radiofrequency device treatment; TempSure firm

Outcome Measures

Primary Outcome Measures

1. Histology of Biopsy [Up to 30 days post last treatment]

   Samples will be assessed independently and may be assessed for normal structures, cell viability, vascular injury, and overall morphologic traits, injury, and any indications of the healing response.

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years to 55 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• A healthy male or female between the age of 18 - 55 years old.

• Willing to receive treatments with the TempSure device and are willing to have biopsies taken from a control site and the treatment area.

• Understands and accepts obligation not to receive any other procedures on the treatment area through the length of the study.

• Understands and accepts the obligation and is logistically able to be present for all visits.

• Is willing to comply with all requirements of the study and sign the informed consent document.

Exclusion Criteria:

• Is pregnant or of childbearing potential and not using medically effective birth control, or has been pregnant in the last 3 months, currently breast feeding or planning a pregnancy during the study.

• The subject is currently enrolled in an investigational drug or device trial or has received an investigational drug or been treated with an investigational device within in the area to be treated 6 months prior to entering this study.

• The subject has a cut, wound, or infected skin on the area to be treated.

• The subject is on local, oral, or systemic anesthetic agents.

• The subject has any condition or is in a situation which in the investigators opinion may put the subject at significant risk, may confound study results or may interfere significantly with the subject's participation.

• The subject is currently enrolled in an investigational drug or device trial, or has received an investigational drug or been treated with an investigational device within in the area to be treated 6 months (or at the discretion of the Investigator) prior to entering this study.

Cautionary Criteria:

• The subject has any embedded electronic device that gives or receives a signal, the device should be turned off or removed prior to treatment.

• The subject has an embedded pacemaker or implantable cardioverter defibrillator (ICD), the client's cardiologist must be consulted prior to treatment.

NOTE: This device has not been tested on patients implanted with electronic devices that receive or emit signals, such as: Pacemakers, Implantable Cardiac Defibrillators (ICD), or Cardiac Resynchronization Therapy (CRT) devices.

• If the neutral pad would need to be placed on a subject that has a metal plate, rod, or any metal implant that could conduct heat from the Smart Handpiece or surgical handpiece.

• The subject is allergic to adhesives, such as glues on medical tape, they should be alerted that a rash may occur on the neutral pad site and an over the counter solution may be used to treat the area.

• The subject is allergic to gold, such as the metallic covering of the TempSure handpieces.

• The subject is allergic to corn, such as the corn derivative ingredient in Parker Aquasonic Gel.

• If the subject has an unhealthy expectation of the results - this is not plastic surgery and all subject should be fully informed of the treatment's expected results.

• The subject has nerve insensitivity to heat in the treatment area.

• The subject has severe laxity or sagging that causes redundant folds of tissue or hanging skin in the area to be treated - this treatment will be ineffective.

• The subject has used Accutane (Isotretinoin) six to twelve months prior to treatment, as this can thin the skin and make it brittle.

• Studies of the use of the RF generator on subjects that have any of the following conditions is unknown:

• Autoimmune Disease

• Diabetic

• Herpes Simplex

• Use caution when treating areas that have scars, tattoos, permanent makeup, and permanent brows.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Bass Plastic Surgery PLLC	New York	New York	United States	10065
2	Aesthetic Pavilion	Staten Island	New York	United States	103206

Sponsors and Collaborators

• Cynosure, Inc.

Investigators

• Study Director: Jennifer Civiok, Cynosure, Inc.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Cynosure, Inc.
• ClinicalTrials.gov Identifier: NCT04584099
• Other Study ID Numbers: CYN20-FIRM-HISTO
• First Posted: Oct 12, 2020
• Last Update Posted: May 31, 2022
• Last Verified: May 1, 2022

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: Yes
• Product Manufactured in and Exported from the U.S.: Yes

Study Results

No Results Posted as of May 31, 2022