跳至主要内容
临床试验/KCT0005981
KCT0005981招募中未知

A 24 weeks, randomized, double-blind, placebo-controlled human trial to evaluate the efficacy and safety of Allium fistulosum L. root extract on improvement of child height growth

Daejeon Korean Medicine Hospital of Daejeon University0 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
5(Year) 至 12(Year)(—)
性别
All

入选标准

  • 1) Children before adolescence, 3~ 25 percentile based on 2017 Korea standard growth chart percentile
  • 2) Spontaneously agreed to participate in the study by the patients and legal guardians or parents

排除标准

  • 1) Participants who have taken Hormone replacement therapy or calcitonin, Phosphonate, growth hormone within 6 month prior to the screening examination
  • 2) Participants with a clinically significant disease requiring treatment (i.e., acute or chronic cardiovascular system, endocrine system, immune system, respiratory system, kidney and urinary system, neuropsychiatric system, musculoskeletal inflammation, inflammatory disease, blood and tumor disease, gastrointestinal disease, etc.)
  • 3) Participants who take medicine or health functional food for improvement of child height growth within 3 month prior to the screening examination
  • 4) Participants with a history of antipsychotic medication use within 3 months prior to the screening examination
  • 5) Participantts who have participated in other clinical trials within 3 months prior to the screening examination
  • 6) Participants who are judged ineligible to participate in the trial by the principal investigator for other reasons, including laboratory test outcomes

研究者

发起方
Daejeon Korean Medicine Hospital of Daejeon University

相似试验

进行中(未招募)
不适用
A 24 week, randomized, double-blind, placebo-controlled, multicenter study to evaluate the efficacy and safety of 18 MCG of Tiotropium inhalation capsules administered by Handihaler® once-daily plus PRN Albuterol (Salbutamol) vs. placebo plus PRN Albuterol (Salbutamol) in Chronic Obstructive Pulmonary Disease subjects naive to maintenance therapy. - N/AChronic Obstructive Pulmonary Disease
EUCTR2006-006276-38-PTBoehringer-Ingelheim436
进行中(未招募)
不适用
A 24 week, randomized, double-blind, placebo-controlled, multicenter study to evaluate the efficacy and safety of 18 MCG of Tiotropium inhalation capsules administered by Handihaler® once-daily plus PRN Albuterol (Salbutamol) vs. placebo plus PRN Albuterol (Salbutamol) in Chronic Obstructive Pulmonary Disease subjects naive to maintenance therapy. - N/AMedDRA version: 8.1Level: LLTClassification code 10009033Term: Chronic obstructive pulmonary diseaseChronic Obstructive Pulmonary Disease
EUCTR2006-006276-38-NLBoehringer-Ingelheim436
招募中
不适用
Effect of medicinal herb aqueous extract on height growth in childre
CTRI/2022/10/046687Korea Medicine Research Institute
进行中(未招募)
不适用
A 24 week, randomized, double-blind, placebo-controlled, multicenter study to evaluate the efficacy and safety of 18 MCG of Tiotropium inhalation capsules administered by Handihaler® once-daily plus PRN Albuterol (Salbutamol) vs. placebo plus PRN Albuterol (Salbutamol) in Chronic Obstructive Pulmonary Disease subjects naive to maintenance therapy. - N/AMedDRA version: 8.1Level: LLTClassification code 10009033Term: Chronic obstructive pulmonary diseaseChronic Obstructive Pulmonary Disease
EUCTR2006-006276-38-BESCS Boehringer Ingelheim Comm.V436
进行中(未招募)
1 期
A 24 week, randomized, double-blind, placebo-controlled, multicenter study to evaluate the efficacy and safety of 18 MCG of Tiotropium inhalation capsules administered by Handihaler® once-daily plus PRN Albuterol (Salbutamol) vs. placebo plus PRN Albuterol (Salbutamol) in Chronic Obstructive Pulmonary Disease subjects naive to maintenance therapy. - N/AMedDRA version: 8.1 Level: LLT Classification code 10009033 Term: Chronic obstructive pulmonary diseaseChronic Obstructive Pulmonary Disease
EUCTR2006-006276-38-GBBoehringer Ingelheim Limited436