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临床试验/JPRN-jRCT1031230422
JPRN-jRCT1031230422招募中2 期

Single-center exploratory study: Evaluation of therapeutic impact GLP-1 a gonist on glucose and lipid metabolism and fatty liver disease in obesity u sing genomic information

Kitamoto Takumi0 个研究点目标入组 50 人开始时间: 2023年10月24日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 18age old 至 < 75age old(—)
性别
All

入选标准

  • 1) Obese patients with a BMI of 30.0 kg/m2 or higher who have glucose intolerance, dyslipidemia, and fatty liver disease, as defined by the Japan Society for the Study of Obesity
  • 2) Patients who are at least 18 years old and less than 75 years old at the time of consent
  • 3) Patients who have been fully informed of the study and who have given written consent of their own free will after sufficient understanding of the study

排除标准

  • Persons who meet any of the following conditions are not eligible
  • 1) Secondary obesity (symptomatic obesity) 2)Patients with a history of wasting disease or condition (severe infection, invasive surgery, malignancy, severe trauma, hyperthyroidism, etc.) that causes extreme weight loss within the past 6 months from the date of consent
  • 3) Patients with severe diabetes mellitus with an H bA1c of 10% or higher
  • 4)Patients with severe hypertension (systolic blood pressure > 180 mmHg)
  • 5) Patients with severe cardiopulmonary, renal, or hepatic dysfunction that is not an indication for exercise therapy
  • 6) Patients with serious musculoskeletal disorders that are not indications for exercise therapy
  • 7) Patients with psychiatric disorders that are difficult to manage
  • 8) Patients who are pregnant, possibly pregnant, within 28 days postpartum, or lactating
  • 9) Patients who are unable to obtain written consent or who do not understand the outline or purpose of the study
  • 10) Other patients who are deemed by the investigator or sub investigator to be unsuitable for the safe conduct of the study

研究者

发起方
Kitamoto Takumi

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