JPRN-UMIN000016673招募中未知
Establishment of a new diagnostic classification for UC patients using the intestinal flora pattern analysis - Establishment of a new diagnostic classification for UC patients using the intestinal flora pattern analysis
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 入组人数
- 200
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 15years-old 至 ot applicable（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •Patient who were judged to be exclusive by investigators
研究者
相似试验
进行中（未招募）
不适用
Pregnancy outcome prediction study 2ISRCTN12181427Cambridge University Hospitals NHS Foundation Trust12,150
招募中
不适用
Improved characterisation of the clinical phenotype of Hereditary Motor Sensory Neuropathy of neuronal type with onset of symptoms in early childhood, especially with respect to disease progression with age and the incidence of such complications as foot deformity, contractures, scoliosis and respiratory involvement - an observational study.Hereditary motor sensory neuropathy of neuronal type with onset in early childhoodHuman Genetics and Inherited Disorders - Other human genetics and inherited disordersNeurological - Other neurological disordersACTRN12605000128695The Children's Hospital at Westmead20
招募中
Unknown
Development of a Scoring System for the Diagnostic Evaluation of Asian Patients with HFpEFheart failure with preserved ejection fractionheart failureJPRN-jRCT1030230465Obokata Masaru750
招募中
不适用
Standard Diagnostic Algorithms to Identify Patients with Inflammatory Bowel Disease In Korean National Health Insurance DatabaseDiseases of the digestive systemKCT0003168Kyung Hee University Hospital61,200
进行中（未招募）
1 期
Definition of the clinicla manifestation variability, response to treatment and natural history in Pearson and Kearns-Sayre syndromePearson and Kearns-Sayre syndrome.MedDRA version: 20.1Level: PTClassification code 10058799Term: Mitochondrial encephalomyopathySystem Organ Class: 10010331 - Congenital, familial and genetic disordersMedDRA version: 20.1Level: PTClassification code 10051403Term: Mitochondrial DNA deletionSystem Organ Class: 10010331 - Congenital, familial and genetic disordersMedDRA version: 20.0Level: LLTClassification code 10074070Term: Mitochondrial encephalopathySystem Organ Class: 10010331 - Congenital, familial and genetic disordersEUCTR2019-003028-19-ITIRCCS, OSPEDALE PEDIATRICO BAMBINO GESÙ DI ROMA27