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Clinical study of acupuncture point embedding combined with Canna edulis RS3 resistant starch in treatment of abdominal obesity with metabolic syndrome

Clinical study of acupuncture point embedding combined with Canna edulis RS3 resistant starch in treatment of abdominal obesity with metabolic syndrome

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088262
Enrollment
Unknown
Registered
2024-08-14
Start date
2022-06-21
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Abdominal obesity with metabolic syndrome

Interventions

Acupoint embedding combined with Canna edulis RS3 resistant starch:Acupoint embedding combined with Canna edulis RS3 resistant starch treatment

Sponsors

Qian Xi Nan Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-65 years. 2. No limitation of ethnic groups. 3. Both sexes. 4. Confirmed abdominal obesity patients with metabolic syndrome: (1) abdominal obesity: the abdominal circumference must reach: male =90cm, female =80cm; (2) Two of the following four indicators must be achieved, namely: (1) have been diagnosed with diabetes and treatment, and (or) fasting blood glucose =6.1 mmol/L or 2 h after glucose loading blood glucose =7.8 mmol/L; Hypertension: Hypertension has been diagnosed, and (or) increased blood pressure: systolic blood pressure =130 mmHg or diastolic blood pressure =85 mmHg; ? Fasting triglyceride =1.70 mmol/L; ? Fasting high-density lipoprotein < 1.04mmol /L. 5. Patients who meet the above diagnostic criteria for MS, are receiving hypoglycemic, hypertensive, lipid-lowering drug treatment, and can stop the above treatment. 6. Have communication and cognitive ability, can adhere to long-term medication. 7. Volunteer to join the experiment.

Exclusion criteria

Exclusion criteria: 1. Those who do not meet the above diagnosis; 2. Those who are in pregnancy and lactation; 3. Those who are participating in other clinical trials; 4. Those who are using weight loss products or drugs; 5. Those with serious heart, lung, kidney, blood system diseases and mental disorders; 6. Those who do not follow the doctor's advice and do not cooperate in examination and treatment; 7. Allergic constitution and allergic to the test drugs; 8. Participating in nutritional intervention studies; 9. Use antibiotics or take probiotics or other prebiotic preparations within 3 months of recruitment.

Design outcomes

Primary

MeasureTime frame
blood lipids;blood pressure;fasting blood-glucose;abdomen circumference;body composition;hip circumference;

Countries

China

Contacts

Public ContactBin Zhou

Qian Xi Nan Hospital of Traditional Chinese Medicine

1021707720@qq.com+86 859 228 0849

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026