跳至主要内容
临床试验/NCT04440722
NCT04440722暂停不适用

Prospective Observational Study and Biobank in All Persons Referred to Center of Gender Identity Odense University Hospital (CKIO)/Body Identity Clinic

Odense University Hospital1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2020年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
暂停
入组人数
100
试验地点
1
主要终点
Hormone levels

研究概览

简要总结

Prospective observational study and biobank in all persons referred to CKIO

  • Patient involvement and quality of life
  • Population characteristics regarding hormone levels, safety parameters and clinical outcome before and after gender affirming hormone treatment.

详细描述

This is a prospective observational cohort study including all patients referred to the Center of Gender Identity Odense. The purpose is to follow patients yearly to observe patient reported outcomes and control the quality and effects of the clinical treatment.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All Individuals with gender dysforia who are referred to Center of Gender Identity Odense

排除标准

  • °There are no exclusion criteria

结局指标

主要结局

Hormone levels

时间窗: Every 52 weeks

Blood samples

Patient reported outcomes (PRO)

时间窗: Every 52 weeks

Questionnaires

Safety parameters

时间窗: Every 52 weeks

Blood samples

次要结局

  • Body weight(Every 52 weeks)
  • Spirometry(Every 52 weeks)
  • Blood pressure(Every 52 weeks)
  • Body mass index(Every 52 weeks)
  • Hair cortisol(Every 52 weeks)
  • Cortisol metabolism(Every 52 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Marianne Andersen

Consultat, Dr Med, professor

Odense University Hospital

研究点 (1)

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