Skip to content

Study on the Efficacy and Safety of Pulsed Ultra-Short Wave Therapy for Obesity with Abnormal Glucose Metabolism

Study on the Efficacy and Safety of Pulsed Ultra-Short Wave Therapy for Obesity with Abnormal Glucose Metabolism

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122775
Enrollment
Unknown
Registered
2026-04-17
Start date
2026-04-20
Completion date
Unknown
Last updated
2026-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity accompanied by abnormal glucose metabolism

Interventions

Treatment group:Using an ultrashort wave therapy device, treat the trunk area. Set the pulse mode and the peak power within the range of 300-500W. Each treatment lasts for 20 minutes. Administer the t

Sponsors

shandong provinvial third hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Age is between 20 years and 60 years; (2) Meet any of the following criteria for obesity or overweight: 1) 28 kg/m^2 = 90 cm for men and >= 85 cm for women; (3) Have impaired fasting glucose with a fasting blood glucose level greater than 6.1 mmol/L or have type 2 diabetes with a glycated hemoglobin level less than 7.5% and have not taken any hypoglycemic drugs; (4) Understand the research procedures and voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Individuals with allergic constitution or a history of gastrointestinal diseases within the past two months; 2. In the acute phase of inflammation; 3. Within 4 weeks prior to screening, having received any medication or treatment that might affect the intestinal flora, such as probiotics or antibiotics; 4. Type 1 diabetes, gestational diabetes, or special types of diabetes; 5. Diabetic patients using any hypoglycemic drugs and those with a glycated hemoglobin level > 7.5%; 6. Having experienced acute diabetic complications within 3 months prior to screening or having severe chronic diabetic complications; 7. Complicated with hypertension, polycystic ovary syndrome, hyperlipidemia, and those whose medication dosage is unstable within 8 weeks before enrollment, and the investigator judges that their treatment drug dosage may be adjusted during the study period; 8. With poor blood pressure control, that is, systolic blood pressure (SBP) > 150 mmHg and/or diastolic blood pressure (DBP) > 95 mmHg (patients with SBP 500 mg/dL (5.65 mmol/L) and/or total cholesterol (TC) > 250 mg/dL (6.45 mmol/L); 10. Complicated with hyperthyroidism or hypothyroidism; 11. Having experienced major diseases within 6 months prior to screening, or any situation that the investigator deems may interfere with the test results or having concurrent diseases; 12. With liver diseases, such as cirrhosis, active hepatitis, or ALT and AST levels higher than 2.5 times the upper limit of normal; severe kidney diseases, eGFR < 45 mL/min/1.73 m^2; 13. Within 4 weeks prior to screening or expected to use drugs that may significantly affect weight, blood sugar, and lipid metabolism, such as various weight loss drugs, steroid hormones, immunosuppressants, etc., with metal foreign bodies in the body, implanted devices such as cardiac pacemakers or insulin pumps, etc.; 14. Patients with other mental disorders who cannot cooperate or refuse to cooperate; or other situations deemed unsuitable for the study by the investigator.

Design outcomes

Primary

MeasureTime frame
Weight;

Secondary

MeasureTime frame
Fasting blood glucose,Fasting insulin;

Countries

China

Contacts

Public ContactXinfeng bai

Shandong Provincial Third Hospital

baixf871025@163.com+86 531 8165 6993

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026