跳至主要内容
临床试验/CTRI/2025/07/091162
CTRI/2025/07/091162招募中不适用

Clinical,Biochemical,genetic profile and gender identity pattern in Disorders of sex development

Department Of Endocrinology1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年7月28日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
1
主要终点
To identify proportion of patients in whom a pathogenic or likely pathogennic variant is idenitfied explaining the DSD phenotype

研究概览

简要总结

To study clinical and biochemical parameters in patients with Disorders of sex development and correlate them with genetic analysis and find discrepancies if any.This could help in more accurate diagnosis and gender assignment . Early appropriate diagnosis would aid in  future therapies and genetic counselling .

研究设计

研究类型
Observational

入排标准

年龄范围
1.00 Day(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • 46 XX and 46 XY DSD with genital ambiguity,proximal or midshaft hypospadias,Apparent female genitalia with clitoromegaly,Female phenotype with primary amenorrhoea,Children with inguinal or labial mass,Posterior labial fusion and common urogenital sinus.

排除标准

  • Sex chromosomal DSD like Turner syndrome and Klinefelter syndrome.
  • Ambiguous genitalia due to maternal androgen exposure ,maternal virilizing ovarian or adrenal tumour.

结局指标

主要结局

To identify proportion of patients in whom a pathogenic or likely pathogennic variant is idenitfied explaining the DSD phenotype

时间窗: Baseline

次要结局

  • To find any discrepancy in assigned gender at birth & gender identity pattern in adolescense

研究者

申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Aravind kumar

Madurai Medical college

研究点 (1)

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