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临床试验/NCT01907464
NCT01907464已完成不适用

Physiopathology of Bone Loss in Young Patient With Anorexia Nervosa

University Hospital, Montpellier2 个研究点 分布在 1 个国家目标入组 320 人开始时间: 2011年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
320
试验地点
2
主要终点
Dual-X-ray absorptiometry (DEXA)

研究概览

简要总结

Nutritional deprivation of adolescent girls with anorexia nervosa (AN) reduces the bone mass acquisition. A better understanding of this process would improve the medical treatment of bone alteration and its long-term consequences.

160 patients (age < 38 yr) with AN and 160 age-matched controls (CON) will be enrolled in this study. The areal bone mineral density (aBMD) will be determined using dual-X-ray absorptiometry. Calciotropic hormones, bone turnover markers will be concomitantly evaluated.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
None

入排标准

年龄范围
14 Years 至 38 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • Informed Consent
  • Health Insurance regimen or benefit from an health insurance regimen
  • Aged from 14 to 38 years old
  • No pregnant
  • Specific inclusion criteria for patient:
  • Patient suffering from anorexia nervosa defined by criteria of Diagnostic and Statistical Manual of Mental Disorders (DSM-IV)
  • Specific inclusion criteria for controls:
  • Normal menstrual cycles,
  • No lifetime history of eating disorders,
  • BMI between 18 and 25 kg/m²

排除标准

  • use of treatments may be modify bone mass (bisphosphonates,…)
  • Disease or treatment may be induce osteoporosis
  • In exclusion period in relation with another study
  • Law protected subject

研究组 & 干预措施

Patients with anorexia nervosa

Experimental

This arm is the experimental arm composed of patients

干预措施: clinical parameters description (Other)

Patients with anorexia nervosa

Experimental

This arm is the experimental arm composed of patients

干预措施: para clinical parameters description (Other)

Patients with anorexia nervosa

Experimental

This arm is the experimental arm composed of patients

干预措施: hormonal parameters dosing (Other)

Patients with anorexia nervosa

Experimental

This arm is the experimental arm composed of patients

干预措施: bone modeling markers dosing (Other)

controls subjects

Active Comparator

This arm is composed of healthy volunteers

干预措施: clinical parameters description (Other)

controls subjects

Active Comparator

This arm is composed of healthy volunteers

干预措施: para clinical parameters description (Other)

controls subjects

Active Comparator

This arm is composed of healthy volunteers

干预措施: hormonal parameters dosing (Other)

controls subjects

Active Comparator

This arm is composed of healthy volunteers

干预措施: bone modeling markers dosing (Other)

结局指标

主要结局

Dual-X-ray absorptiometry (DEXA)

时间窗: at Day 0 (time of the inclusion visit)

The primary outcome is to model the bone mass acquisition in young women with anorexia nervosa.

次要结局

  • Biological parameters identification(At day 0 (time of the inclusion visit))
  • clinical parameters identification(At Day 0 (at time of the the inclusion visit))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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