跳至主要内容
临床试验/KCT0012241
KCT0012241招募中不适用

A 12-week, Randomized, Double-blind, Placebo-controlled Human Study to Evaluate the Safety and Efficacy of the Probiotic Combination of L. reuteri CKDB010 and B. longum NBM7-1 (CKDB-344) for Improving Muscle Strength and Physical Function

Woosuk University Korean Medicine Medical Center0 个研究点目标入组 100 人开始时间: 2026年6月19日最近更新:
适应症
干预措施

试验速览

阶段
不适用
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
主要目的
Supportive Care

入排标准

年龄范围
50(Year) 至 85(Year)(—)
性别
All

入选标准

  • •Subjects who voluntarily provided written informed consent after receiving a full explanation of the study
  • •Male and female adults aged 50 to 85 years at the time of providing written informed consent
  • •Subjects with a body mass index (BMI) =18.5 kg/m² and <30.0 kg/m²
  • •Subjects with handgrip strength below the age-specific reference value
  • •Subjects with a Short Physical Performance Battery (SPPB) score >9

排除标准

  • •Subjects with a history of fragility hip fracture
  • •Subjects with any of the following conditions, medical histories, or surgical histories: musculoskeletal disorders, neurological disorders, uncontrolled hypertension, uncontrolled diabetes mellitus, taking medications for the treatment of psychiatric disorders, gastrointestinal disorders that may affect the ingestion or absorption of the investigational product, etc
  • •Heavy smokers
  • •Subjects with hypersensitivity to any component of the investigational product or a history of allergy that, in the investigator's judgment, makes participation in the study inappropriate
  • •Subjects who participated in another clinical study and received an investigational product, investigational food, investigational medical device within 3 months prior to screening
  • •Subjects who, in the investigator's judgment, are considered unsuitable for participation in the study for any other reason
  • •Pregnant or lactating women
  • •Women of childbearing potential and men who are unable or unwilling to use appropriate methods of contraception during the study period

研究组 & 干预措施

Dietary Supplement : Test Product: Capsules containing CKDB-344

干预措施: Dietary Supplement : Test Product: Capsules containing CKDB-344

研究者

发起方
Woosuk University Korean Medicine Medical Center

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