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Real World Study : Changes in related risk factors after combined treatment with semaglutide in Chinese obese population with cardiovascular high-risk factors

Real World Study : Changes in related risk factors after combined treatment with semaglutide in Chinese obese population with cardiovascular high-risk factors

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400081406
Enrollment
Unknown
Registered
2024-02-29
Start date
2023-12-01
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Cardiovascular metabolic disorders

Interventions

Combination therapy with semaglutide treatment.:NA

Sponsors

First Affiliated Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 78 Years

Inclusion criteria

Inclusion criteria: 1.Fully understand the purpose and requirements of this study, sign the informed consent form, and exhibit good compliance. 2.Patients meeting the following criteria: a. Obesity or overweight individuals aged =18 years: BMI = 23 kg/m^2 (Asian criteria) Abdominal obesity: Male waist circumference = 90 cm or female = 85 cm, waist-to-hip ratio = 1.0 b. Patients with comorbidities such as hypertension, diabetes or impaired glucose tolerance, insulin resistance, hyperlipidemia, hyperuricemia, and hyperhomocysteinemia. 3.History of, currently receiving, or voluntarily requesting treatment with semaglutide.

Exclusion criteria

Exclusion criteria: 1. Contraindications for the use of semaglutide include conditions such as medullary thyroid carcinoma in patients with multiple endocrine neoplasia syndrome type 2. 2. Patients with a history of allergy to GLP-1 analogs. 3. Active enteritis or gastritis; gastrointestinal ulcers or bleeding; post-gastrointestinal surgery. 4. Pregnancy or lactation. 5. Other malignant diseases affecting patient survival, such as severe autoimmune diseases. 6. Special dietary habits, such as vegetarianism. 7. Situations where the investigator deems recruitment inappropriate. 8. Patients currently participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Body Weight;BMI;Waist circumference,;waist-to-hip ratio;systolic blood pressure;diastolic blood pressure;fasting blood glucose;2-hour postprandial blood glucose;glycated hemoglobin;total cholesterol;triglycerides;low-density lipoprotein;high-density lipoprotein;uric acid;Homocysteine;

Secondary

MeasureTime frame
Time to achieve 5% and 10% weight loss from the start of treatment;MACE;

Countries

China

Contacts

Public ContactAilan Chen

Datansha Campus, The First Affiliated Hospital of Guangzhou Medical University

1228327958@qq.com+86 137 1919 8832

Outcome results

None listed

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