跳至主要内容
临床试验/NCT03921918
NCT03921918已完成不适用

Evaluation of Fluid-Filled Expression Core Technology Study - I

Medela AG2 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2019年5月8日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Medela AG
入组人数
26
试验地点
2
主要终点
Recording all Adverse Events

研究概览

简要总结

A functional model of a fluid-filled, smaller dead volume breast pump has been developed in order to more closely mimic the breastfeeding infant. The technology of fluid-filled pumping has been tested in one prior clinical study and has now progressed to a complete prototype with which the user can assemble, pump, disassemble, clean and reuse.

详细描述

Current breast pumps function in a way that is different to breastfeeding. These include the seal to the breast, the movement of the nipple, the sensations of warmth and moisture, the variability in frequency, and the strength of the applied vacuum. During breastfeeding the mother's nipple and the infant's mouth form a chamber that is a fluid-filled, no dead volume system, which is needed to create a working vacuum to remove milk from the breast. There is no air visible in the natural system according to ultrasound measurements. This is unlike breast pumps which use an air-filled, large dead volume system, to create a working vacuum. Therefore, a functional model of a fluid-filled, smaller dead volume breast pump has been developed in order to more closely mimic the breastfeeding infant. The technology of fluid-filled pumping has been tested in one prior clinical study and has now progressed to a complete prototype with which the user can assemble, pump, disassemble, clean and reuse.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Subject ≥ 18 years old
  • Infant is ≥1 and ≤6 month old
  • Subject and baby are healthy according to self-declaration in the "Mother and infant health questionnaire"
  • Subject is predominantly breastfeeding (80% of all feeds, i.e. ≤150 ml formula/day or equal representative amount of solid food)
  • The subject agrees to pump or feed the last time a minimum of 2 hours (hr) before the start of the pumping session at the study site
  • The subject agrees to photographs/3 D scan of the breast and upper body (no face),
  • The subject agrees to a video while pumping
  • The subject signs the informed consent documentation
  • Subject agrees that a maximum of 2 male team members can be present in the room to conduct the usability part of the study
  • The mother accepts that the pumped milk in visit 2 must be donated to the study i.e. cannot be fed to the baby

排除标准

  • The subject has a nipple size ≥ 21 mm
  • Mastitis (any breast within two weeks prior to enrolment)
  • Engorgement (any breast within two weeks prior to enrolment).
  • Case of current infection as self-declared in the Mother and infant health questionnaire

结局指标

主要结局

Recording all Adverse Events

时间窗: 3 months

Recording all AE and evaluating the (time of) occurrence, type, seriousness, expectedness, relatedness, and outcome of the adverse events

Observing pump performance

时间窗: 3 months

Measuring milk flow volume including time to first ejection.

次要结局

  • Measureing user acceptance(3 months)

研究者

发起方
Medela AG
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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