Status:
WITHDRAWN
The Effect and the Pharmacogenomics Study of Liraglutide in Obese Patients
Lead Sponsor:
Xiangya Hospital of Central South University
Conditions:
Obesity
Eligibility:
All Genders
18-65 years
Phase:
PHASE2
Brief Summary
This studay evaluates the effect of liraglutide in the treatment of obese patients ande the influence of genetic factors on the curative effect.Half of participants will receive Liraglutide alone,whil...
Detailed Description
Background:The rapid growth of obese or overweight people in the world has become a major social problem. Obese often associated with kinds of metabolic disorders, especially type 2 diabetes, and Lira...
Eligibility Criteria
Inclusion
- Patients aged 18 to 65 years (to the date of screening)；
- 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).
- 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.
- Weight stable for more than 3 months (weight fluctuations \<5%).
Exclusion
- Pregnant female.
- 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.
- Severe cardiovascular and cerebrovascular diseases (heart failure, myocardial infarction, acute hemorrhagic or ischemic encephalopathy), pulmonary heart disease or pulmonary insufficiency, renal failure, severe hepatitis.
- Combined with acute complications of diabetes such as ketoacidosis, lactic acidosis, hyperosmolar state of diabetes.
- Nearly a month had surgery, trauma, infection and so on.
- Limb deformity incomplete, difficult to accurately determine the height, weight and other physical indicators.
- Poor medication compliance or serious side effects (severe rash, syncope, etc.).
Key Trial Info
Start Date :
December 1 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2021
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT04839237
Start Date
December 1 2017
End Date
December 1 2021
Last Update
April 9 2021
Active Locations (1)
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1
Xiangya Hospital of Central South University
Changsha, Hunan, China, 410008