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临床试验/NCT01400659
NCT01400659已完成4 期

The PIZZA-Salami Trial: Monocentric Randomised Cross-over Study of Carb Counting vs. Carb Plus Fat/Protein Counting Based Insulin Bolus Used for Sensor-augmented Continuous Subcutaneous Insulin Infusion (CSII) in Pediatric Patients

Kinderkrankenhaus auf der Bult0 个研究点目标入组 42 人开始时间: 2009年3月1日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
42
主要终点
CGM-Glucose Area Under the Curve

研究概览

简要总结

The Pizza-Salami-Study aims to investigate the efficacy of carbohydrate plus fat/protein (CFP) counting compared with carbohydrate (CARB) counting using normal and dual-wave bolus in sensor-augmented pump therapy in children and adolescents with type 1 diabetes. For fat/protein counting the model used by Pankowska et al. will be applied.

详细描述

This is a prospective, international multi-centre, open randomized clinical trial to assess whether the use of Paradigm REAL-Time System from the onset of Type 1 Diabetes (T1D) leads to a better glycaemic control after 12 months of T1D compared with the use of Paradigm 515/715 insulin pump combined with conventional Self-Monitoring Blood Glucose finger-sticks in paediatric patients. Total randomized treatment duration of the study for a patient will be 12 months with an optional phase of follow-up of 3 months.Patients eligible according to inclusion and exclusion criteria will be randomized to one of the two treatment groups. A total of 160 patients will be recruited. Each subject will participate in the study for 15 months, which includes 12 months of treatment and 3 months of follow-up. Each patient is asked to use either the Paradigm REAL-Time System that provides a combination of insulin pump and the Real-Time continuous glucose monitoring or Paradigm 515/715 insulin pump combined to conventional SMBG finger-sticks. Main time-points of assessments are at baseline (within one month after T1D onset) and 12 months thereafter. In total, there will be 6 study visits at the local site. During study, patients will regularly attend the outpatient clinic according to local Standard care, i.e. every 8±2 weeks.

研究设计

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

入排标准

年龄范围
6 Years 至 21 Years(Child, Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients with type 1 diabetes
  • •Age 6 - 21 years
  • •Diabetes duration > 1 year
  • •Treatment with pump therapy (CSII) > 3 months
  • •Written informed consent by patients and parents
  • •Patients must be willing to wear a glucose sensor for two days and to perform capillary blood glucose measurement twice a day
  • •Patients must be willing to performed all study procedures

排除标准

  • •Language barriers
  • •Eating disorders
  • •Pregnancy
  • •Drug abuse
  • •Patient refutes participation or study procedures

研究组 & 干预措施

CARB Counting

Active Comparator

For CARB counting, insulin dose will be calculated according to the carbohydrate content of the test meal (1 carb unit = 10 g carbohydrate). The insulin-to-carbohydrate ratio will be applied according to the current individual therapy of the patient.

干预措施: CFP counting (Procedure)

CFP counting

Active Comparator

For CFP counting, insulin dose will be calculated according the carbohydrate content (1 carb unit = 10 g carbohydrate) as well as fat/protein content (1 FPU = 100 kcal from fat and protein) of the meal. The insulin-to-carbohydrate ratio will be applied according to the current individual therapy of the patient. The insulin-to-FPU ratio is the same as the insulin to carb ratio.

干预措施: CARB counting (Procedure)

结局指标

主要结局

CGM-Glucose Area Under the Curve

时间窗: 6 hours after the test meal

CGM = Continuous Glucose Monitoring

次要结局

  • Time of glucose nadir(6 hours after the test meal)
  • hyperglycemia (6h-AUC >180 mg/dl)(6 h after the test meal)
  • frequency and amount of interventional hypoglycemic therapy(6 h after the test meal)
  • frequency of adverse events (incl. SAE)(during hospitalization period of the study)

研究者

发起方
Kinderkrankenhaus auf der Bult
申办方类型
Other
责任方
Sponsor

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