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临床试验/NCT01267526
NCT01267526已完成不适用

"Easypod™ Connect Registry": A Canadian, Multi-centre, Observational Registry to Study Adherence and Long Term Outcomes of SAIZEN® in Pediatric Subjects Using Easypod™ Auto-injector

Merck KGaA, Darmstadt, Germany1 个研究点 分布在 1 个国家目标入组 205 人开始时间: 2011年5月31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
205
试验地点
1
主要终点
Mean percent of adherence by subject over a period of time

研究概览

简要总结

This is a Canadian, Multicentre, Observational Registry to study Adherence and Long Term Outcomes of Therapy in paediatric subjects using Easypod™ electromechanical device for growth hormone treatment from hospital and to assess the level of adherence of subject receiving SAIZEN® via Easypod™ .

详细描述

Subjects will be enrolled in a multicenter, longitudinal observational registry. Parents/subjects will provide their Informed Consent/assent to upload their data for populationbased analyses and optionally to adhere to a patient adherence support program designed to improve their adherence and, ultimately, clinical outcomes. Adherence data will be primarily derived from the Easypod™ device combined with physician data entry of outcome measures. Data will be collected retrospectively and prospectively. This will allow the establishment of adherence profiles and explore the hypothesis that patient adherence support programs improve adherence and subsequent clinical outcomes. Collected data will be also analyzed in a multinational pooled analysis of comparable national studies.

Primary Objective:

  • To assess the level of adherence of subjects prescribed SAIZEN® via easypod™

Secondary Objectives:

  • To describe the impact of adherence on clinical outcomes for subject prescribed SAIZEN via easypod™
  • To identify adherence subject profiling

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
2 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Prescribed SAIZEN® via the easypod™ auto-injector (SAIZEN® Health Canadian approved indications: Growth Hormone Insufficiency or Deficiency, Turner's Syndrome, Chronic Renal Failure, Small for Gestational Age
  • Under 18 years of age, or over 18 without fusion of growth plates
  • Parent's or legal guardian's written informed consent, given before entering data into the registry, with the understanding that the subject or parent/legal guardian may withdraw consent at any time without prejudice to future medical care. If the child is old enough to read and write, a separate assent form will be given as defined by Health Canada regulations. Adult consent is defined at 18+ in the province of Quebec, 16+ in the remainder of Canada.

排除标准

  • Subjects taking growth hormone in whom growth plates have fused (i.e. for taking growth hormone for its metabolic effects)
  • Contra-indications to SAIZEN® as defined in SAIZEN® Canadian Product Monograph.
  • Use of an investigational drug or participation in another interventional clinical study

结局指标

主要结局

Mean percent of adherence by subject over a period of time

时间窗: At least 6 months and up to 5 years

Adherence will be defined as 86 percent adherent at one year based on prescribed therapy.

次要结局

  • Correlation of adherence and growth outcome after each year of SAIZEN® treatment with easypod™(At least 6 months and up to 5 years)
  • Subject adherence profile based on age, gender, indication, self-injection or not, time on treatment(At least 6 months and up to 5 years)
  • Impact of patient adherence support programme on adherence and outcomes for subjects using easypod™(At least 6 months and up to 5 years)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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