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Individualized multidisciplinary weight management in patients with metabolic syndrome

An observation study for clinical indicators improvement from individualized multidisciplinary weight management in patients with metabolic syndrome

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900022948
Enrollment
Unknown
Registered
2019-05-04
Start date
2019-06-01
Completion date
Unknown
Last updated
2022-05-02

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

Conditions

Metabolism Syndrome

Interventions

Case series:individualized multidisciplinary weight management

Sponsors

Nanjing Medical University Affillated Wuxi People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. According to the IDF definition of MS in 2009 combined with the national standards of CDS,abdominal obesity (waist circumference >= 90cm for men and >= 85cm for women) as the prerequisite with two or more of the following metabolic abnormalities: Elevated triglyceride level (>= 1.7 mmol/L) or receipt of specific treatment for this lipid abnormality; Reduced HDL-C level (= 130mmHg or diastolic BP >= 85mmHg) or current treatment for hypertension or previously diagnosed hypertension; Elevated PG level (fasting PG >= 5.6mmol/L or 2 h postprandial PG >= 7.8 mmol/L) or previously diagnosed diabetes mellitus. 2. Aged 18 to 65 years, male or female; 3. Women in childbearing age agree to use contraceptive measures during the test; 4. Patients can understand and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Secondary obesitysuch as hypothyroidism,Cushing's syndrome, or long-term use of drugs that lead to obesity. 2. Chronic diseases of heart, brain, liver, kidney and other organs that require a special diet or affects exercise 3. Rheumatic and immune diseases, hematological diseases or a history of malignancy. 4. Female during pregnancy or lactation. 5. Unable, unwilling or unwilling to comply with the research requirements, including lifestyle modification, return visit, and subject responsibility.

Design outcomes

Primary

MeasureTime frame
Height;Weight;Waist circumference;Hip circumference;Neck circumference;Calf circumference;Thigh circumference;Blood pressure;Blood lipid;Blood sugar;OGTT;Islet function;Human body composition analysis;Cardiopulmonary exercise test;

Secondary

MeasureTime frame
fat accumulation in pancreas;fat accumulation in liver;Anxiety scale;Depression scale;Impact of weight on quality of life questionnaire-Life version;

Countries

China

Contacts

Public ContactWu Wenjun

Nanjing Medical University Affillated Wuxi People's Hospital

wuwenjung@163.com+86 15358008856

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 26, 2026