Clinical trial Recruiting at 1 site Interventional Ages 25 to 40 Women only

Ultrasound treatment for insulin resistance in women with central obesity

Official title: Effect of Ultrasound Cavitation on Insulin Resistance in Patients with Central Obesity in Female

Run by Cairo University · NCT06729203 · Data updated 2026-11-12

This study tests if combining ultrasound treatments with exercise and a low-calorie diet can help women aged 25 to 40 with central obesity improve their insulin resistance and body shape.

More Central Obesity trials

Quick facts

Study typeInterventional
Ages25 Years to 40 Years
SexWomen only
Enrollment52 (estimated)
SponsorCairo University
Academic / other
Locations1 site (Giza, Giza Governorate)
StatusRecruiting
StartedDecember 1, 2024
Main results expectedFebruary 1, 2025
Study endsDecember 1, 2025
Registry record updatedDecember 11, 2024
Trial IDNCT06729203 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are sedentary women aged 25 to 40 with a BMI between 30 and 35 kg/m2 and diagnosed with insulin resistance.

Probably not a fit

Patients with diabetes, metabolic disorders, or those on weight-loss medications are unlikely to benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the effects of ultrasound cavitation combined with aerobic exercise and a low-calorie diet on insulin resistance and body contouring in women aged 25 to 40 with central obesity. Participants will undergo ultrasound treatments while following a structured exercise and dietary program. The primary focus is to assess changes in insulin resistance, measured by HOMA-IR, as well as improvements in body composition. The study aims to provide clearer evidence on the efficacy of ultrasound cavitation in managing obesity-related insulin resistance.

Why it matters

Potential benefit: If successful, this approach could offer a non-invasive method to improve insulin sensitivity and aid in weight management for women with central obesity.

How similar studies have gone: While there is limited evidence on the effects of ultrasound cavitation on insulin resistance, similar studies have shown promise in body contouring and metabolic improvements.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Female subjects with central obesity.
* Female participants aged between 25 to 40 years.
* Body Mass Index (BMI) ranged from 30 to 35 kg/m2 as high BMI indicates more obesity and central obesity.
* Waist circumference greater than 88 cm, indicative of abdominal obesity.
* Diagnosed with insulin resistance (HOMA-IR \> 2.9).
* Sedentary lifestyle, defined as engaging in less than 150 minutes of moderate-intensity physical activity per week.
* Willingness to provide informed consent and comply with study procedures.

Exclusion Criteria:

* • Subjects diagnosed with DM (HbA1c more than 6.5%).

  * History of metabolic disorders such as type 1 diabetes or thyroid disorders.
  * Subjects with BMI less than 30 kg/m2.
  * Subjects diagnosed with heart disease, liver as well as kidney diseases.
  * Subjects who take oral contraceptives.
  * Subjects with gestational Diabetes.
  * Pregnant or breastfeeding women were excluded from the study.
  * Use of weight-loss medications or supplements within the past six months.
  * Previous surgical procedures for weight loss or body contouring.
  * Contraindications to ultrasound therapy (e.g., metal implants in the abdomen, active skin infections).
  * Participation in another clinical trial within the last three months.

Where it's running

  • Cairo University
    Giza, Giza Governorate, Egypt
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.