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Cystic Fibrosis Related Bone Disease: the Role of CFTR

2020年3月24日 更新者:Melissa Susan Putman、Massachusetts General Hospital
The purpose of this study is to determine whether ivacaftor, a recently FDA-approved CFTR potentiator, improves bone micro-architecture and strength in patients with cystic fibrosis with at least one G551D CFTR mutation.

研究概览

地位

完全的

详细说明

Ivacaftor, a CFTR potentiator, has recently been FDA approved for the treatment of cystic fibrosis in patients with at least one G551D CFTR mutation. Given the possible role of CFTR in bone, we hypothesize that this medication may also improve bone health in CF patients. The purpose of this study is to test this hypothesis using high resolution peripheral quantitative computed tomography, a research tool that measures bone micro-architecture and volumetric bone density and has the ability to detect small changes in bone that might otherwise be missed with standard bone imaging techniques such as bone density testing.

研究类型

观察性的

注册 (实际的)

79

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Massachusetts
      • Boston、Massachusetts、美国、02114
        • Massachusetts General Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

6年 至 75年 (孩子、成人、年长者)

接受健康志愿者

是的

有资格学习的性别

全部

取样方法

非概率样本

研究人群

Subjects with CF will be recruited from the Cystic Fibrosis Centers at Children's Hospital Boston and Massachusetts General Hospital. Healthy subjects will be a community sample recruited from nearby communities.

描述

COHORT 1

Inclusion Criteria:

  • Age 6 to 75 years old
  • Established diagnosis of CF with at least one abnormal G551D-CFTR allele
  • Eligibility for and intent to start treatment with ivacaftor or started treatment with ivacaftor within previous 6 months

Exclusion Criteria:

  • Psychiatric or mental incapacity that would preclude subject from assenting to study participation
  • Current pregnancy
  • History of organ transplantation
  • History of Burkholderia dolosa infection

COHORT 2:

Subjects will be grouped by gender, age and race to match subjects in Cohort 1 within two years. Pubertal subjects will be matched by Tanner stage.

Inclusion Criteria:

  • Age 6 to 75 years old
  • Established diagnosis of CF

Exclusion Criteria:

  • Psychiatric or mental incapacity that would preclude subject from assenting to study participation
  • Current pregnancy
  • History of organ transplantation
  • History of Burkholderia dolosa infection

COHORT 3:

Subjects will be grouped by gender, age and race to match subjects in Cohort 2 within two years. Pubertal subjects will be matched by Tanner stage.

Inclusion criteria:

  • Age 6 to 75 years old
  • Clinically stable, deemed able to complete the screening, baseline, and scheduled study visits.

Exclusion criteria:

  • History of significant cardiac, renal, pulmonary, hepatic, or malignant disease, current alcohol or illicit drug abuse, or major psychiatric disorder
  • Current diagnoses known to affect bone metabolism, including cystic fibrosis, osteoporosis, amenorrhea >3 months (in menstruating women who are not taking oral contraceptives or have an IUD), hyperthyroidism, diabetes, hyperparathyroidism, Paget's disease, kidney stones, chronic inflammatory diseases, malabsorptive disorders, malnutrition, prolonged immobility, and skeletal dysplasias
  • History of a non-digital fracture in the previous 6 months, history of one pathologic fracture, or greater than four total lifetime non-digital fractures
  • Cumulative lifetime use of oral glucocorticoids for greater than 2 months
  • Current or prior use of medications known to affect bone metabolism including hormone replacement therapy, anti-estrogens, bisphosphonates, calcitonin, fluoride, lithium, suppressive doses of levothyroxine, or anticonvulsants.
  • Pregnancy
  • BMI less than 18.5 or greater than 30 kg/m2 in subjects 18 years and older, or BMI less than 5th or greater than 95th percentile in subjects under the age of 18 years.
  • Any medical or psychiatric condition or situation that would compromise subject safety, informed consent/assent, treatment compliance, follow-up measurements, or data quality

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
Subjects with CF taking ivacaftor
Subjects with CF ages 6 to 75 years old who will be or have started taking ivacaftor within the previous 6 months
Subjects with CF not taking ivacaftor
Subjects with CF ages 6 to 75 years old who will not be taking ivacaftor, matched for age, race, and gender with cohort 1
Healthy subjects
Healthy subjects with no medical conditions known to affect bone between the ages of 6 to 75 years old, matched for age, race, and gender with cohort 2.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Bone Microarchitecture and Strength Measures of the Radius and Tibia
大体时间:Baseline and 24 months
Change in cortical volumetric bone mineral density at the radius
Baseline and 24 months

次要结果测量

结果测量
措施说明
大体时间
Areal Bone Mineral Density as Measured by DXA
大体时间:Baseline and 24 months
Change in PA spine bone mineral density
Baseline and 24 months
Bone Turnover Markers
大体时间:Baseline and 24 months
Change in osteocalcin
Baseline and 24 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Joel Finkelstein, MD、Massachusetts General Hospital

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2012年4月1日

初级完成 (实际的)

2018年5月1日

研究完成 (实际的)

2020年2月1日

研究注册日期

首次提交

2012年3月2日

首先提交符合 QC 标准的

2012年3月6日

首次发布 (估计)

2012年3月9日

研究记录更新

最后更新发布 (实际的)

2020年4月1日

上次提交的符合 QC 标准的更新

2020年3月24日

最后验证

2020年3月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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