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临床试验/NCT00046501
NCT00046501已完成3 期

Morning LANTUS v. Intermediate-acting Insulin 2x/Day as Basal Insulin in a Multiple Daily Inj. w/ Humalog in Adolescents w/ Type 1 Diabetes Mellitus: an Active-controlled, Open, Randomized, Gender-stratified, Two-arm, Parallel-group Study

Sanofi2 个研究点 分布在 1 个国家目标入组 250 人开始时间: 2002年11月1日最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
Sanofi
入组人数
250
试验地点
2
主要终点
to measure change in glycemic control as measured by hemoglobin A1c (A1c).

研究概览

简要总结

The purpose of the study is to compare the effect in blood sugar control between Lantus and twice daily intermediate acting insulins (NPH or Lente) when used as the basal insulin in a multiple daily injection setting with fast acting insulin (Lispro)

研究设计

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

入排标准

年龄范围
9 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Type 1 diabetes treated with insulin only for at least 1 year,
  • with a Tanner stage of ≥ 2,
  • had evidence of decreased insulin secretory capacity (fasting C-peptide concentration ≤0.5 mmol/L) and 7.0%≤A1c≤9.5% at screening.
  • The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

排除标准

  • 未提供

结局指标

主要结局

to measure change in glycemic control as measured by hemoglobin A1c (A1c).

时间窗: from baseline to endpoint (last available post-treatment assessment)

次要结局

  • Change in 8-point blood glucose profiles for weekdays, weekends, and weekday/weekend combined(from baseline to endpoint)
  • Change in lipids (total cholesterol [TC], high-density lipoprotein cholesterol [HDL], low-density lipoprotein cholesterol [LDL], and triglycerides [TGs])(from baseline to endpoint)
  • Adverse events (AEs)(from the informed consent signature to the end of the study)
  • Change in A1c(from baseline to individual study time points)
  • Percentage of subjects achieving an A1c ≤7.0; percent of preteens (12 years and below) achieving 8%; teens (13-18 years) achieving 7.5%(During the study conduct)
  • Change in urinary spot random microalbumin-to-creatinine (A/C) ratio(from baseline to endpoint)
  • Change in average basal insulin doses(from baseline to endpoint)
  • Change in glucose(from baseline to endpoint)
  • Occurrence of hypoglycemia(from the informed consent signature to the end of the study)
  • Clinical values: physical examination, vital signs, change in age-adjusted body mass index (BMI)(from the informed consent signature to the end of the study)
  • Change in fasting self-monitored blood glucose (SMBG) for weekdays, weekends and weekday/weekend combined(from baseline to endpoint)

研究者

发起方
Sanofi
申办方类型
Industry

研究点 (2)

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