Safety and Effectiveness of High Frequency Electrocautery for Abdominal Fat Reduction

Chinese Medical Association

Status: Active, not recruiting

Conditions: BMI

Treatments: Device: Placebo; Device: treatment of radiofrequency technology

Study type: Interventional

Funder types: NETWORK

Identifiers

NCT06850246

03010240620

Details and patient eligibility

About

The goal of this clinical trial is to learn if the intervention of radiofrequency technology can help treat abdominal fat hypertrophy and skin laxity in adults. The main questions it aims to answer are

• Does radiofrequency technology lower the abdominal subcutaneous adipose tissue height by ultrasound measurement?
• Does radiofrequency technology improve abdominal circumference data and lower the number of times participants need to use a rescue inhaler.

Researchers will compare the treatment side to the non-treatment side to see if radiofrequency technology works to treat abdominal fat hypertrophy and skin laxity?

Participants will:

• Accept the treatment of radiofrequency technology every week for 10 weeks.
• Visit the clinic 1 month and 3 months after the treatment ends for checkups and tests.

Enrollment: 30 estimated patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Voluntarily sign the informed consent form;
2. Age 18 to 65 years old (including 18 and 65 years old), male or female;
3. The body mass index (BMI) is in the range of 22 ~ 35 (kg/m2) (including the cut-off value);
4. Maintain a stable weight and lifestyle (including calorie intake and exercise) throughout the clinical study period and within 6 months after the end of the study;
5. Non-pregnant and breastfeeding women who have no pregnancy plan and voluntarily take effective contraceptive measures during the screening period and the whole trial period, and have no sperm or egg donation plan.

Exclusion criteria

1. Patients who gained or lost more than 2.5 kg of weight during the study;
2. Patients who have used weight loss drugs or participated in weight loss-related programs within 6 months of the start of the study;
3. Have received or are about to receive surgery or liposuction in the abdomen, or have received lipolytic drugs injected in the abdomen, or have received abdominoplasty or cryo lipolysis;
4. History of abdominal/waist-related trauma or scar;
5. Patients with excessive accumulation of abdominal skin affecting the operation;
6. Implantation of metal-related articles in the abdomen;
7. Patients suffering from severe systemic diseases that are life-threatening (such as cardiac insufficiency, renal insufficiency, etc.);
8. Those who are equipped with dentures, pacemakers, or other internal metal implants (such as metal IUD rings, etc.);
9. Local skin infection and open skin injury;
10. Have a history of eating disorder or eating disorder;
11. Pregnant or breastfeeding women.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Single Group Assignment

Masking: Triple Blind

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30 participants in 2 patient groups, including a placebo group

radiofrequency technology

Experimental group

Description:

First, the frequency of 470 kHz was selected, and the CRT resistance probe was performed for deep fat management operation for 10 minutes, and then the CET capacitive mode 470 kHz was selected for superficial fat operation for 6 minutes. Then, select the 940 kHz frequency CET capacitance probe for epidermal tightening operation for 4 minutes. The temperature is set by the energy value. In CRT mode, the energy value is set to 70, and it can reach above 42 ℃ within one minute. In CET mode, the energy value setting is adjusted to 75. The operation mode is to gradually raise the temperature to the midline after partially increasing the temperature at the side of the waist. The technique is mainly to move in a circle and lift to the midline.

Treatment:

Device: treatment of radiofrequency technology

Placebo

Placebo Comparator group

Description:

Under the condition that the machine is not turned on, the treatment is performed in the same operation time, mode and treatment area of the treatment group.

Treatment:

Device: Placebo