DRKS00034523招募中不适用
Genotype-phenotype association study in patientswith genetic obesity - PhaeGAdi
niversitätsklinikum Ulm - Sektion Pädiatrische Endokrinologie und Diabetologie0 个研究点目标入组 50 人开始时间: 2024年6月26日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 50
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
- one 至 one(—)
- 性别
- All
入选标准
- •Patients with monogenic obesity
- •Patients with syndromic obesity
- •Patients with extreme early childhood obesity or adolescents with extreme obesity and suspected new, previously unknown form of genetic obesity
排除标准
- •Inability to give consent, e.g. due to lack of German language skills
研究者
相似试验
已完成
不适用
Association between genotype and clinical course of amyotrophic lateral sclerosisamyotrophic lateral sclerosisJPRN-UMIN000030729Toranomon Hospital Kajigaya
已完成
不适用
Investigation on associations of genotype and phenotype in patients with DysfibrinogenemiaD68.2Hereditary deficiency of other clotting factorsDRKS00014093Klinikum der Johann Wolfgang Goethe-Universität Frankfurt am Main69
招募中
不适用
Genetics and its influence on physical characteristics in Indian Patients with Congenital Adrenal Hyperplasia due to 21-α hydroxylase deficiency.CTRI/2019/04/018430A
已完成
不适用
Association study of genome for common disease, especially circulatory diseases, renal disases and hypertension.JPRN-UMIN000013004Yokohama City University Graduate School of Medicine1,000
已完成
不适用
Study on genotype and phenotype relation by genome analysis of responsible gene region in SMASpinal Muscular AtrophyJPRN-UMIN000040095Institute of Medical Genetics, Tokyo Women's Medical University50
