Belly fat battle: which body sculpting method lowers inflammation?
NCT ID NCT07307898
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compares two non-invasive body treatments—ultrasound cavitation and whole-body electrical muscle stimulation—to see which better reduces inflammation in people with central obesity (excess belly fat). Sixty adults aged 18-50 with a large waistline will be assigned to one of the treatments. Researchers will measure changes in inflammatory markers and waist size over the study period.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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60 people
The number who actually took part.
- Started
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Sep 2024
- Expected to finish
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Jan 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 50 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults aged 18-50 years. * Individuals diagnosed with central obesity, defined as a waist circumference greater than 102 cm in men and 88 cm in women. * Participants with a stable body weight for at least three months prior to the study. * No engagement in regular physical activity or weight loss programs in the past six months. * Willingness to adhere to study protocols and attend all scheduled sessions. Exclusion Criteria: * Individuals with chronic diseases other than obesity-related conditions, such as cardiovascular disease, diabetes, or severe hypertension. * Pregnant or lactating women. * Individuals with implanted electronic devices (e.g., pacemakers). * Participants with dermatological conditions or skin infections in the treatment area. * Individuals undergoing medication that may affect fat metabolism or inflammatory markers.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Cairo University
Cairo, Qalyubia Governorate, 13611, Egypt
More trials for these conditions
Other studies related to the condition(s) this trial covers.