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临床试验/NCT07301437
NCT07301437尚未招募4 期

A Real-world Study of Liraglutide Alone and in Combination With Orlistat for Weight Loss in Overweight/Obese Patients.

The Fourth Affiliated Hospital of Zhejiang University School of Medicine0 个研究点目标入组 120 人开始时间: 2026年5月1日最近更新:
干预措施

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
120
主要终点
weight loss

研究概览

简要总结

To evaluate the differences in weight loss between liraglutide monotherapy and combined with orlistat in overweight/obese patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • BMI: ≤ 35 kg/m² and ≥ 30 kg/m², or ≥ 27 kg/m² and having at least one obesity-related complication (such as hypertension, type 2 diabetes, dyslipidemia)
  • Voluntarily sign the informed consent form, agreeing to cooperate in completing the 24-week treatment and follow-up.
  • No severe cognitive impairment or mental illness, and able to understand and comply with the research requirements.

排除标准

  • Allergy to liraglutide, orlistat or excipients
  • Severe liver and kidney dysfunction: ALT or AST> three times the upper limit of normal, or eGFR <30 mL/min
  • Thyroid diseases: Personal or family history of medullary thyroid cancer, or uncontrolled hyperthyroidism/hypothyroidism
  • Gastrointestinal diseases: Having gastrointestinal surgery within 3 months, or inflammatory bowel disease or active gastric and duodenal ulcers
  • Pregnant or lactating women
  • Others: Type 1 diabetes, malignant tumors, severe cardiovascular diseases (such as NYHA IV).

研究组 & 干预措施

experimental group

Experimental

干预措施: liraglutide combined with orlistat (Drug)

control group

Active Comparator

干预措施: liraglutide monotherapy (Drug)

结局指标

主要结局

weight loss

时间窗: 6 months

次要结局

未报告次要终点

研究者

发起方
The Fourth Affiliated Hospital of Zhejiang University School of Medicine
申办方类型
Other
责任方
Sponsor

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