Trim II for Noninvasive Lipolysis and Circumference Reduction of Abdomen.

Not Applicable

Completed

• Conditions: Circumference Reduction of Abdomen
• Interventions: Device: Trim II

• Registration Number: NCT05398159
• Lead Sponsor: InMode MD Ltd.

Brief Summary

At least 90 female and male subjects, from 6 investigational sites, aged 18-70 seeking non-invasive lipolysis and circumference reduction of abdomen will be enrolled. Eligible subjects will receive 3 bi-weekly treatments (once in 2 weeks) with Trim II hands-free applicator belt according to the study protocol.Study duration for each subject is approximately 6 months (including screening, 3 treatments and 2 follow-up visits at 1 and 3 months post last treatment).

Detailed Description

The goal of this prospective study is to evaluate Safety and Efficacy of Trim II for Non-invasive Lipolysis and Circumference Reduction of Abdomen.

The main questions are :

* Efficacy of the Trim II treatment for lipolysis and abdominal circumference reduction.

* Safety of the Trim II treatment for lipolysis and abdominal circumference reduction

Eligible subjects will receive 3 bi-weekly treatments (once in 2 weeks) with Trim II hands-free applicator belt according to the study protocol.

Study Timeline

• Study Start: 2021-03-10
• Study First Submitted: 2022-05-17
• Study First Submitted QC: 2022-05-25
• Study First Posted: 2022-05-31
• Primary Completion: 2022-10-30
• Study Completion: 2022-10-30
• Results First Submitted: 2022-12-01
• Status Verified: 2024-06
• Results First Submitted QC: 2024-06-10
• Last Update Submitted: 2024-06-10
• Results First Posted: 2024-06-11
• Last Update Posted: 2024-06-11

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 75

Inclusion Criteria

• Female and male subjects, aged 18-70.
• BMI≤ 30.
• Subjects seeking non-invasive lipolysis and circumference reduction of abdomen
• Female should not be pregnant or lactating and must be either post-menopausal, surgically sterilized, or using a medically acceptable form of birth control at least 3 months prior to enrolment (i.e., oral contraceptives, contraceptive implant, barrier methods with spermicide or abstinence).
• In addition, negative urine pregnancy test as tested before each treatment and at the last visit for women with childbearing potential (e.g. not menopause).
• General good health confirmed by medical history and skin examination of the treated area.
• The subjects should understand the information provided about the investigative nature of the treatment, possible benefits and side effects, and sign the Informed Consent Form, including permission to use photography.
• The subjects should be willing to comply with the study procedure and schedule, including the follow up visits, and will refrain from using any other abdominal treatment methods during the entire study period.

Exclusion Criteria

• • Active electrical implant/device in any region of the body, including pacemaker or internal defibrillator
• Permanent implant in the treated area such as metal plates, screws or silicon, metal piercing or other.
• Current or history of skin cancer, or current condition of any other type of cancer, or pre-malignant moles.
• Severe concurrent conditions, such as cardiac disorders, sensory disturbances, epilepsy, uncontrolled hypertension, and liver or kidney diseases.
• History of skin disorders, keloids, abnormal wound healing, as well as very dry and fragile skin.
• History of bleeding coagulopathies or use of anticoagulants except for low-dose aspirin.
• Patients with history of diseases stimulated by heat, such as recurrent Herpes Simplex in the treatment area, may be treated only following a prophylactic regimen.
• Impaired immune system due to immunosuppressive diseases such as AIDS and HIV or use of immunosuppressive medications.
• Pregnancy and nursing.
• Poorly controlled endocrine disorders, such as Diabetes, or thyroid dysfunction and hormonal virilization.
• Isotretinoin (Accutane) within last 6 months.
• Any active condition in the treatment area, such as sores, Psoriasis, eczema, and rash, open lacerations, abrasions or lesions, infection in the area to be treated.
• Any surgical procedure in the treatment area within the last 12 months or before complete healing.
• Having received treatment with light, laser, RF, or other devices in the treated area within 2-3 weeks for non-ablative procedures, and 6-12 weeks for ablative fractional laser resurfacing (according to treatment severity) prior to treatment, except special recommendations.
• Use of non-steroidal anti-inflammatory drugs (NSAIDS, e.g., ibuprofen-containing agents) one week before and after each treatment session, as per the practitioner's discretion.
• As per the investigator's discretion, refrain from treating any condition which might make it unsafe for the patient.
• Participated in another investigational drug or device study or have completed the follow-up phase for any previous study less than 30 days prior to the first evaluation in this study.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
treatment	Trim II	3 bi-weekly treatments

Primary Outcome Measures

Name	Time	Method
Evaluation of Change in Abdomen Circumference Using Tape Measurements in cm at the 3 Months Follow-up Visit Comparing to Baseline.	3 months	Efficacy of the Trim II treatment for lipolysis and abdominal circumference reduction.; Evaluation of change in abdomen circumference using tape measurements in cm at the 3 months follow-up visit comparing to baseline.; Success criteria: Statistically significant reduction in abdominal circumference tape measurements at the 3 months follow-up visit compared to baseline
Safety of the Trim II Treatment for Lipolysis and Abdominal Circumference Reduction.	3 months	Number of participants with incidence of Treatment-Emergent Adverse Events \[Safety and Tolerability\]) will be followed throughout the whole study. Observation, assessment, and recording of potential reactions by the investigator.; Evaluations will be done immediately after each treatment and at the follow-up visits. The frequency, severity, and causality of reactions will be recorded.

Secondary Outcome Measures

Name	Time	Method
Subject's Satisfaction With Study Treatment at 3 Months Follow-up Visit.	3 months	Subject's satisfaction with the therapy results was evaluated through the Subject Satisfaction Questionnaire (5-point scale). The higher the score the better the outcome. 2-Very satisfied, 1-satisfied, 0-indifferent, -1 disappointed, -2- very disappointed
Change in Abdominal Fat Thickness Measured by Ultrasound Imaging (USI) at the 3 Months Follow-up Visit Comparing to Baseline.	3 months	Success criteria: statistically significant change in fat thickness of the abdomen (treatment) area measurements at the 3 months follow-up visit compared to baseline.
Percentage of Participants With Baseline and 3 Month Abdomen Photographs Correctly Identified by Two Blind Evaluators	3 months	Success criteria: Correct identification of baseline and 3-month follow-up visit photographs of the abdomen (treatment) area in at least 70% of treated subjects by two blinded evaluators.
Treatment Comfort During the Study Treatment.	Immediately post each treatment once in 2 weeks for 6 weeks	Average of comfort post treatment evaluated using the Therapy Comfort Questionnaire. Scored from-2 to +2. The higher the score the better the outcome. Average value is calculated

Trial Locations

Locations (5)

H/K/B Cosmetic Surgery; 🇺🇸 Huntersville, North Carolina, United States

Bucky Body Center; 🇺🇸 Philadelphia, Pennsylvania, United States

Tennessee Clinical Research Center; 🇺🇸 Nashville, Tennessee, United States

Dallas Plastic Surgery Institute; 🇺🇸 Dallas, Texas, United States

Refresh Dermatology; 🇺🇸 Houston, Texas, United States