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临床试验/NCT02368496
NCT02368496已完成不适用

Parenteral Nutrition and Bone Trophicity

Hospices Civils de Lyon4 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2014年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
17
试验地点
4
主要终点
Bone mineral density (BMD) and Bone mineral contain (BMC) height z-score at baseline

研究概览

简要总结

Recent progress in parenteral nutrition has contributed to improve vital prognosis and to reduce morbidity in patients with severe intestinal failure.

Currently, home parenteral nutrition is the only alternative to prolonged hospitalization for those patients. However, long-term parenteral nutrition can result in complications especially in bone, such as osteopenia or osteomalacia, then increasing the risk of fractures. Children are especially at risk because of bone growth and peak mineralization acquisition during puberty.

Moreover, frequency and risk factors of those complications are not well documented for children.

Dual-energy X-ray Absorptiometry (DXA) is considered as the golden standard for bone mineralization measurement. In pediatrics, this technique has some limits such as the underestimation of Bone Mineral Density (BMD) in short stature, the overestimation of the BMD in tall children, and the inability to distinguish cortical from trabecular bone or to evaluate the bone microarchitecture.

HR-pQCT, High Resolution peripheral Quantitative Computed Tomography enables noninvasive assessment of bone microarchitecture (virtual bone biopsy) using a radiation similar to DXA. However this technique has never been validated in patients with long-term parenteral nutrition.

During the usual follow-up of the patients, HR-pQCT will be the only exam which will come in addition to the routine medical tests.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
9 Years 至 30 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Patient who's receiving a long-term parenteral nutrition (over 2 years)
  • Patient between 9 and 30 years of age (children big enough to stay immobile for 3 min during the measurement)
  • Affiliation to the Social Security System
  • Informed consent form signed by parents and assent given by the patient

排除标准

  • Patient presenting a bone disease which is not directly related to the parenteral nutrition.
  • Long-term corticotherapy ( over 6 months of therapy)
  • Inability to keep the leg or the arm immobile for 3 min
  • Patient not affiliated to a Social Security System
  • Patient participating to another interventional study
  • Pregnant patient or patient who desires pregnancy
  • All situation that the physician estimated that is not compatible with the study

结局指标

主要结局

Bone mineral density (BMD) and Bone mineral contain (BMC) height z-score at baseline

时间窗: J0 (baseline)

BMD and BMC z scores (after correction for the height) will be measured by High Resolution peripheral Quantitative Computed Tomography (HR-pQCT) and compared to those measured in a control group (healthy subjects matched on age and sex). The same measurements will be also compared with those obtained by Dual-energy X Ray (DXA) but in this case each subject will be considered as his own control.

次要结局

  • Trabecular and cortical BMD z score(J0 (baseline))
  • BMD and BMC height z score after 1 year of parenteral nutrition (PN)(1 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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