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临床试验/NCT06673160
NCT06673160招募中不适用

Pumping to Up Maternal Milk Production for Preterms (PUMMPP)

University of Alabama at Birmingham1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2025年6月11日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
70
试验地点
1
主要终点
Volume of expressed breastmilk

研究概览

简要总结

The goal of this clinical trial is to learn about the effect of breast-pumping frequency on breast milk supply/ volume in mothers of preterm infants. The main question it aims to answer is:

- What effect does pumping frequency have on breast milk supply.

Researchers will compare breastmilk supply of mothers who pump every 2 hours to the supply of those who pump every 3 hours to see if there is a difference in the amount of breastmilk they produce.

Participants will be assigned to either pump every 2 hours or every 3 hours and record how many milliliters of breastmilk they produce daily for the first 28 days of their baby's life.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
— 至 28 Days(Child)
性别
All
接受健康志愿者

入选标准

  • Inborn infants <32 weeks gestation
  • Out-born infants transferred to our facility <48hours of life
  • Infants <1500 grams at birth
  • Infants whose parents/ guardians have provided legal consent for study participation

排除标准

  • Infants with birthing persons' that are severe/critically ill
  • Birthing persons of infants <18 years old
  • Infants with terminal illness or decision to withhold or limit support
  • infants with major congenital anomalies, chromosomal disorders, or congenital infections

研究组 & 干预措施

Pumping every 2 hours

Experimental

Mothers of patients in this group will be assigned to pump/ express breastmilk every 2 hours.

干预措施: Pumping every 2 hours (Behavioral)

Pumping every 3 hours

Active Comparator

Mothers of patients in this group will be assigned to pump/ express breastmilk every 3 hours.

干预措施: breast pumping every 3 hours (Behavioral)

结局指标

主要结局

Volume of expressed breastmilk

时间窗: From enrollment to 28 days of life

The primary outcome measure will be the volume of expressed breastmilk obtained in mL per day in the group pumping every 2 hours compared the group pumping every 3 hours

次要结局

  • The percentage of donor breast milk feedings(From enrollment to 28 days of life)
  • The time to full feedings(From enrollment to 28 days of life)
  • The number of days alive on full feedings(From enrollment to 28 days of life)
  • Average change in weight(from birth to 36 weeks' corrected gestational age)
  • The number of infants with clinical evidence of feeding intolerance(From enrollment to first 28 days after birth)
  • The number of infants exclusively feeding breastmilk at discharge(From enrollment to hospital discharge)
  • Average change in length(from birth to 36 weeks corrected gestational age)
  • Average change in head circumference(from birth to 36 weeks' corrected gestational age)
  • Number of central line days(In the first 28 days of life)
  • The number of infants receiving any volume of breastmilk at time of discharge(From enrollment to hospital discharge)
  • The Bayley Scales of Infant and Toddler Development (BSID)(From 18-26 months of age)
  • The Bayley Scales of Infant and Toddler Development (BSID)(from 18-26 months of age)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Colm Travers

Associate Professor

University of Alabama at Birmingham

研究点 (1)

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