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Effects of GLP-1 RAs on Weight and Metabolic Indicators in Obese Patients

Effects of GLP-1 RAs on Weight and Metabolic Indicators in Obese Patients

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03671733
Enrollment
150
Registered
2018-09-14
Start date
2018-09-01
Completion date
2022-09-01
Last updated
2021-04-09

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

Conditions

Obesity

Brief summary

This studay evaluates the effect of the glucagon-like peptide-1 (GLP-1) receptor agonist,including Liraglutide,Exenatide and Exenatide Microspheres for Injection,in the treatment of subjects who are overweight or obese.

Interventions

DRUGLiraglutide

The treatment of Liraglutide lasted three months,During the first week: 0.6mg per day, subcutaneous injection;During the second week: 1.2mg per day, subcutaneous injection; From third week onwards, 1.8mg per day, subcutaneous injection.

DRUGExenatide

10mcg once a day for 4 weeks increased to 10mcg twice a day for 8 weeks.

DRUGExenatide Microspheres for Injection

Exenatide 2 mg injection once weekly for 12 weeks.

Sponsors

Xiangya Hospital of Central South University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Patients aged 18 to 65 years (to the date of screening); 2. The newly diagnosed obese patients (BMI greater than 28 kg/m2) or abdominal obesity (male waist circumference is greater than 90cm, female waist is greater than 85cm). 3. Nearly a month have not used weight-related drugs,including various weight-loss drugs,GLP-1 analogs or agonists,metformin, acarbose,insulin,anti hyperthyroid drugs,etc;Or recently used weight-related drugs but the stable dose was more than 1 month,and the drug dose remained constant or decreased during the trial. 4. Weight stable for more than 3 months (weight fluctuations \<5%).

Exclusion criteria

1. pregnant female. 2. Secondary diseases caused by other diseases: including hypothyroidism, increased cortisol, hypothalamic and pituitary lesions caused by obesity, all kinds of drug-induced obesity, and others. 3. Severe cardiovascular and cerebrovascular diseases (heart failure, myocardial infarction, acute hemorrhagic or ischemic encephalopathy), pulmonary heart disease or pulmonary insufficiency, renal failure, severe hepatitis. 4. Combined with acute complications of diabetes such as ketoacidosis, lactic acidosis, hyperosmolar state of diabetes. 5. Nearly a month had surgery, trauma, infection and so on. 6. Limb deformity incomplete, difficult to accurately determine the height, weight and other physical indicators. 7. Poor medication compliance or serious side effects (severe rash, syncope, etc.).

Design outcomes

Primary

MeasureTime frameDescription
Weight Change at 3 monthsbaseline , 3 monthsMeasured in kilograms

Secondary

MeasureTime frameDescription
Change in systolic blood pressurebaseline and 3 monthsMeasured in mmHg
Change in diastolic blood pressurebaseline and 3 monthsMeasured in mmHg
Change in HbA1cbaseline and 3 monthsMeasured in %
Change in plasma glucosebaseline and 3 monthsMeasured in mmol/l
Change in insulinbaseline and 3 monthsMeasured in μU/ml
Change in lipids-total cholesterolbaseline and 3 monthsMeasured in mmol/l
Change in waist circumferencebaseline and 3 monthsMeasured in cm
Change in lipids-high density lipoprotein cholesterolbaseline and 3 monthsMeasured in mmol/l
Change in lipids-triglyceridesbaseline and 3 monthsMeasured in mmol/l
Change in lipids-free fatty acidsbaseline and 3 monthsMeasured in μmol/l
Change in Uric Acidbaseline and 3 monthsMeasured in mmol/l
Change in interleukin-6baseline and 3 monthsMeasured in mmol/l
Change in tumor necrosis factorbaseline and 3 monthsMeasured in mmol/l
Change in lipids-low density lipoprotein cholesterolbaseline and 3 monthsMeasured in mmol/l

Countries

China

Contacts

Primary ContactJing Wu
wujing0731@163.com+86-13574120508

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026