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A Multicenter, Prospective, Observational Study of Liraglutide Injection (Rilupine) in the Treatment of Overweight or Obese Patients

A Multicenter, Prospective, Observational Study of Liraglutide Injection (Rilupine) in the Treatment of Overweight or Obese Patients

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400090984
Enrollment
Unknown
Registered
2024-10-17
Start date
2024-07-19
Completion date
Unknown
Last updated
2024-10-21

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

Conditions

overweight or obese

Interventions

Case series:None

Sponsors

Nanchang First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Age= 18 years old, gender is not limited; (2) Subject 24.0 kg/m2= body mass index (BMI)<28.0 kg/m2 [body mass index BMI=weight (kg)/height 2(m2)] at screening, with at least one weight-related comorbidity, or body mass index (BMI=28.0kg/m2, with or without comorbidities; and stable body weight (less than 5% self-reported weight change within 3 months); (3) Patients with overweight/obesity with comorbidities such as hypertension, diabetes mellitus, and dyslipidemia must meet the relevant disease diagnostic criteria (please refer to the guidelines for the prevention and management of primary hypertension at the national level (2020 edition), the guidelines for the prevention and treatment of type 2 diabetes in China (2020 edition) and the guidelines for the management of blood lipids in China (2023), among which overweight/obesity with diabetes mellitus must have glycosylated hemoglobin (HbA1c) test results within 1 month before enrollment; (4) First treatment with liraglutide injection (rilupine); (5) Voluntarily participate in the study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Personal or family history of medullary thyroid cancer (MTC) or multiple endocrine neoplasia type 2 (MEN2); (2) Have a history of severe allergy to liraglutide or any excipient component of this product; (3) Participation in any other clinical trial currently or within the past 1 month; (4) Not suitable to participate in this study as judged by the investigator.

Design outcomes

Primary

MeasureTime frame
weight;

Secondary

MeasureTime frame
Body mass index;waistline;Hip circumference;Depression Rating Scale (PHQ-9) score;Glycosylated hemoglobin;Fasting blood glucose;Blood pressure;blood lipids;Echocardiographic indicators;Blood glucose 2 hours postprandial;Fasting insulin;Fasting C-peptide;electrocardiogram;Complete blood count;Blood biochemistry;Urinalysis;Markers of heart failure;Serum creatinine;Protein in the urine;

Countries

China

Contacts

Public ContactHu Ling

Nanchang First Hospital

hul@medmail.com+86 139 7007 5119

Outcome results

None listed

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