Comparing electric current techniques for abdominal fat reduction in women
Comparative Acute Effects of the Application of Percutaneous and Transcutaneous Electrolipolysis on the Female Abdominal Contour: a Cross Over Clinical Trial
NA · Universidade Federal de Pernambuco · NCT05973526
This study is testing two different electric current methods to see which one helps women reduce belly fat more effectively.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 20 (estimated) |
| Ages | 18 Years to 35 Years |
| Sex | Female |
| Sponsor | Universidade Federal de Pernambuco (other) |
| Locations | 1 site (Recife, Pernambuco) |
| Trial ID | NCT05973526 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to compare the effects of two techniques, percutaneous and transcutaneous electrolipolysis, on reducing abdominal fat in women. Participants will undergo 12 sessions over 6 weeks, with each session lasting 50 minutes, and their abdominal areas will be randomly assigned to receive one of the two techniques. The study will evaluate the effectiveness of each method in reducing adipose tissue and assess participant comfort during the procedures.
Who should consider this trial
Good fit: Ideal candidates for this study are women with localized abdominal fat and a BMI between 18.5 and 29.9 who are sedentary and not on a supervised diet.
Not a fit: Patients who are smokers, pregnant, or have metabolic disorders or other specified exclusions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a non-invasive and effective method for women to reduce abdominal fat and improve their body contour.
How similar studies have performed: While electrolipolysis has been explored in other studies, this specific comparison of percutaneous versus transcutaneous techniques is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Women between with localized abdominal fat * Body Mass Index (BMI) between 18.5 and 29.9 kg/m2 (adequate weight and overweight) * Who have not undergone any treatment for the condition experienced in the last 6 months * Sedentary * Not on a supervised diet Exclusion Criteria: * Smokers * Alcoholics * Pregnant women * Metabolic and circulatory system disorders * Pacemaker * Metallic implants * Tumors/metastasis * Dermatitis * In treatment with corticosteroids and/or prolonged progesterone * Skin ulcers/lesions * Needle phobia (aichmophobia) * Sensitivity alteration in the region to be treated * Unable to understand the form and/or procedure * Not completing the suggested protocol * Dietary changes during the research
Where this trial is running
Recife, Pernambuco
- Federal University of Pernambuco — Recife, Pernambuco, Brazil (RECRUITING)
Study contacts
- Study coordinator: Rennatha Moura Medeiros
- Email: rennathamedeiros@outlook.com
- Phone: +55 (81) 997166634
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Abdominal Fat, adipose tissue, subcutaneous fat