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临床试验/KCT0009505
KCT0009505招募中未知

A 8 week, Single-center, Randomized, Double-Blind, Placebo-Controlled Clinical Trial for the Evaluation of the Efficacy and Safety of SPB-201on gastric functional

Sungkyunbiotech0 个研究点目标入组 100 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
招募中
发起方
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
19(Year) 至 70(Year)(—)
性别
All

入选标准

  • 1) A person who is 19 years of age or older and 70 years of age or younger
  • 2) A person diagnosed with functional dyspepsia
  • 3) Those who have at least 4 of the 10 symptoms in the GIS questionnaire and have a total score of 12 or more
  • 4) Where it is possible to bring the result of gastroscopy performed within 6 months, and the result sheet determines that there is no organic disease
  • 5) A person who agrees to participate in this human body application test before the human body application test begins and prepares a written consent form.

排除标准

  • 1)Severe cardiovascular system, immune system, respiratory system, gastrointestinal/hepatic and biliary system, kidney and urinary system, nervous system, mental, infectious disease, and malignant tumor can participate in the test at the discretion of the tester.
  • 2)A person who has a history of peptic ulcer or other diseases (such as colostrum disease) that may cause gastrointestinal symptoms within 6 months of visiting 1
  • 3)Those with gastrointestinal surgical history (excluding appendectomy and hemorrhoids)
  • 4)A person with a history of digestive malignancies
  • 5)Those who have taken H2 receptor blockers, anticholinergics (muscarin receptor antagonists), gastrin receptor antagonists, prostaglandin preparations, proton pump inhibitors, gastric mucosa protectors, gastrointestinal motility boosters, and other health-related functional foods within 2 weeks of visit 1
  • 6)A person who has taken drugs that can cause gastritis, such as adrenocorticotropic hormone drugs, nonsteroidal anti-inflammatory drugs, aspirin, erythromycin, and antidepressants, within 2 weeks of visiting 1
  • 7)A person with a history of drug addiction
  • 8) Those with alcohol consumption habits exceeding the average 30g/day for men (about 3 beers and 3 soju) and 20g/day for women (about 2 beers and 2 soju) per week in the drinking habit survey over the past month
  • 9)Patients with uncontrolled hypertension (systolic blood pressure of 160mmHg or diastolic blood pressure of 100mmHg or more, test subjects after 10 minutes of rest)
  • 10)Patients with uncontrolled diabetes (abdominal blood sugar greater than 180 mg/dL)
  • 11)A person whose creatine is more than twice the upper limit of the normal administrative agency
  • 12)Those whose AST (GOT) or ALT (GPT) is at least three times the upper limit of the normal authority
  • 13)Those whose amylase and lipase are more than twice the upper limit of normal levels of the agency (but abnormal values can be excluded at the discretion of the researcher)
  • 14)Those whose TSH is 0.1 µIU/mL or less, or 10 µIU/mL or more
  • 15)Those who are sensitive to or allergic to food ingredients for human application tests
  • 16)Pregnant or nursing mothers or those who plan to become pregnant during the period of this human body application test
  • 17)A person who has participated in other interventional clinical trials (including human application tests) within three months of visiting 1 or plans to participate in other interventional clinical trials (including human application tests) after the start of this human application test
  • 18)A person deemed by a tester to be inappropriate for this human body application test

研究者

发起方
Sungkyunbiotech

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