CTRI/2022/12/048044尚未招募未知
PEDIATRIC CHRONIC KIDNEY DISEASE PROGRAM: IDENTIFICATION OF BIOMARKERS BY SERUM AND URINARY METABOLONOMICS FOR EARLY IDENTIFICATION OF PROGRESSION - CKD metabolomics
ICMR0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
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
入选标准
- •All children of age 2-18 years with diagnosed chronic kidney disease (all stages of CKD). Attempt shall be made to include 50 children in early stages (1-3) and another 50 in late (4-5) stages of CKD.
- •For controls: Healthy age and gender matched children attending outpatients for minor illnesses in a 2:1 ratio of cases and controls. A total of 50 controls shall be enrolled.
排除标准
- •Patient presently having acute kidney injury, any bacterial infections or receiving any immunosuppressants, with structural heart disease or undergoing dialysis will be excluded.
研究者
相似试验
招募中
不适用
Chronic Kidney Disease in Children Prospective Cohort Study (CKiD)Chronic Kidney DiseaseNCT00327860Johns Hopkins Bloomberg School of Public Health1,300
招募中
不适用
A cohort study of pediatric chronic kidney diseaseJPRN-UMIN000015768Japanese Pediatric CKD Study Group400
尚未招募
Unknown
Optimising diagnosis and management of chronic disease in primary care: an implementation study of a clinical decision support software Future Health Today.Renal and Urogenital - Kidney diseaseMetabolic and Endocrine - DiabetesCardiovascular - Coronary heart diseaseStroke - Ischaemicdiabeteschronic kidney diseasecardiovascular diseaseACTRN12623001096640Western Health20
招募中
不适用
Identifying the critically ill paediatric oncology patientpaediatric cancerNL-OMON24811KiKa grant number 2871,500
招募中
不适用
etwork for Early Onset Cystic Kidney DiseasesQ61.1Q61.3Q61.8Q61.9Q87.5Q87.8Q77.2Q77.6Q77.9Polycystic kidney, autosomal recessivePolycystic kidney, unspecifiedOther cystic kidney diseasesCystic kidney disease, unspecifiedOther congenital malformation syndromes with other skeletal changesOther specified congenital malformation syndromes, not elsewhere classifiedShort rib syndromeChondroectodermal dysplasiaOsteochondrodysplasia with defects of growth of tubular bones and spine, unspecifiedDRKS00011003niversitätsklinikum Münster, Klinik für Kinder-und Jugendmedizin, Allgemeine Pädiatrie, Leiter Pädiatrische Nephrologie, Stellvertretender Direktor Allgemeine Pädiatrie500