Validation of the Clinical Value of Interstitial Fluid Biomarkers in Skin

akamura Kenjiro0 个研究点目标入组 60 人开始时间: 2024年1月9日最近更新: 2024年4月23日

适应症

试验速览

暂无简介。

•(1) Patients who are outpatients or inpatients with blood biomarkers (BM) above or below the threshold level established for each disease, or healthy adults with normal BMs.
•(2) Patients who are at least 18 years old and less than 70 years old at the time of consent.
•(3) (Healthy adult group only) Body Mass Index between 18.5 and 25.0
•(4) Patients who can obtain document consent with their own will before any study related procedure

•(1) Those who are unable to undergo blood tests.
•(2) Persons with obvious skin abnormalities (abnormal pigmentation, swelling, wounds, etc.) at the site of interstitial fluid collection (bilateral forearms)
•(3) Patients who have received an injectable medication or vaccination within 1 week.
•(4) (Healthy adult group only) Those who are allergic to inhaled allergens (pollen, house dust, etc.)
•(5) (Healthy adult group only) Those with allergies to food, drugs, metals, etc., and have confirmed exposure to the relevant allergens within 1 week.
•(6) (Healthy adult group only) Those who have suffered a traumatic injury or received invasive treatment within 1 week.
•(7) (Healthy adult group only) Persons who have contracted an infectious disease within 3 weeks
•(8) Persons with hypersensitivity to raw materials (aluminum alloy and polypropylene) used in the research equipment.
•(9) Other persons who are judged to be ineligible by the principal investigators or research assistants.

发起方

akamura Kenjiro