跳至主要内容
临床试验/CTRI/2023/10/059320
CTRI/2023/10/059320尚未招募Unknown

Targeted Next Generation Sequencing based approach to explore potential pathogenic variants in patients with non-syndromic congenital heart defects. - NI

Department of Science and Technology0 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
Unknown
状态
尚未招募

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

  • The study subjects will be pediatric live births and adult patients. The patients will be thoroughly screened for breathing problems, failure to thrive, heart murmur, fatigue, and family history by the cardiologist. Phenotypic data for the affected individuals and their family members will be obtained from the detailed clinical evaluation based on Electrocardiogram, Two-dimensional Echocardiography, cardiac catheterization and surgical findings. Peripheral blood samples from all the participants will be collected in EDTA K2 tubes after informed consent as per the extensive clinical criteria.

排除标准

  • Patients with syndromic congenital heart defects will be excluded from the study.

研究者

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