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临床试验/NCT05614089
NCT05614089已完成4 期

Human Versus Analogue Insulin for Youth With Type 1 Diabetes in Low-Resource Settings: A Randomized Controlled Trial

Jing Luo3 个研究点 分布在 2 个国家目标入组 400 人开始时间: 2023年3月15日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
400
试验地点
3
主要终点
Time-in-serious Hypoglycemia

研究概览

简要总结

The primary objective of this trial is to determine whether insulin glargine reduces the risk of serious hypoglycemia or improves Time in Range at 6 months when compared against standard of care human insulin (e.g. NPH or premixed 70/30) among youth living with type 1 diabetes (T1D) in low resource settings.

详细描述

Long-acting insulin analogues have become a de-facto standard of care for patients with T1D living in high-income countries. Unfortunately, insulin analogues remain unavailable or unaffordable for much of the global population. In both 2017 and 2019, applications to add long-acting insulin analogues to the WHO's Model List of Essential Medicines (EML) were rejected due to insufficient evidence of superiority and an unfavorable cost-effectiveness profile when compared against older, less expensive, human insulins (e.g., NPH insulin and premixed 70/30 insulin). In 2021, long-acting insulin analogues were added to the EML but the decision remains controversial since the WHO concluded that "magnitude of clinical benefit of long-acting insulin analogues over human insulin for most clinical outcomes was small." Moreover, studies that compare long-acting insulin analogues versus human insulins conducted in high-income settings may not generalize to children and young adults living with T1D in very low-resource settings.

To address this unmet need, Pitt has partnered with Brigham and Women's Hospital, The London School of Hygiene and Tropical Medicine, the Clinton Health Access Initiative and Life For a Child to conduct a randomized controlled trial comparing insulin glargine, a long-acting analogue insulin, against intermediate human insulin among 400 children and young adults living with T1D in a lower resource setting.

Note: In preparation for results submission, we made minor changes to the outcomes sections to reflect what is listed in the protocol.

For Primary Outcomes #1 and #2, and Secondary Outcomes #3,#4, #5, #7, #8: we added 12 months measurements (in addition to the 6 months measurement). We updated Secondary Outcome #9 to specify the PedsQL Diabetes Symptoms Score. We added Secondary Outcome #10 to include the PedsQL Diabetes Management Score. We added Secondary Outcome #11 for ITSQ scores.

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
7 Years 至 25 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Children and young adults (age 7-25)
  • Have a clinical diagnosis of type 1 diabetes (T1D)

排除标准

  • Prior use of any insulin analogue
  • Patients (or parents for children <18 years old) who refuse to or cannot provide informed consent
  • Who are currently pregnant or plan to become pregnant over the next year
  • Who have previously used a continuous glucose monitor (CGM) for glucose monitoring
  • Who were first diagnosed with T1D less than 12 months ago
  • Who is diagnosed with severe malnutrition

研究组 & 干预措施

Glargine

Experimental

Insulin glargine (long-acting insulin analogue)

干预措施: Insulin Glargine (Drug)

NPH or premixed 70/30 (human insulin)

Active Comparator

NPH or premixed 70/30 (human insulin)

干预措施: NPH or premixed 70/30 (human insulin) (Drug)

结局指标

主要结局

Time-in-serious Hypoglycemia

时间窗: 6 and 12 months after randomization

% time spent less than 54 mg/dl averaged across all daily measures. For 6-month outcome, these data were averaged across two CGM sensors (placed at 6 and 6.5 months). For 12-month outcome, these data were from one CGM sensor placed at 11.5 months.

Time-in-range (TIR)

时间窗: 6 and 12 months after randomization

% time spent between 70 and 180mg/dl inclusive averaged across all daily measures. For 6-month outcome, these data were averaged across two CGM sensors (placed at 6 and 6.5 months). For 12-month outcome, these data were from one CGM sensor placed at 11.5 months.

次要结局

  • Time-in-hypoglycemia(6 and 12 months after randomization)
  • Time-above-range(6 and 12 months after randomization)
  • Nocturnal Hypoglycemic Events(6 and 12 months after randomization)
  • Glycemic Control (HbA1c)(baseline, 3, 6, 9 and 12 months after randomization)
  • Rate of Severe Hypoglycemic Events(6 and 12 months after randomization)
  • Rate of Diabetic Ketoacidosis (DKA)(6 and 12 months after randomization)
  • Pediatric Quality of Life Inventory 3.2 Diabetes Module (PedsQL 3.2 DM) Diabetes Symptoms Score(Baseline and at 6 and 12 months after randomization)
  • Pediatric Quality of Life Inventory 3.2 Diabetes Module (PedsQL 3.2 DM) Diabetes Management Score(Baseline and at 6 and 12 months after randomization)
  • Insulin Treatment Satisfaction Questionnaire (ITSQ) Scores(Baseline and at 6 and 12 months after randomization)

研究者

发起方
Jing Luo
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Jing Luo

Associate Professor

University of Pittsburgh

研究点 (3)

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