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Completed

NCT Number: NCT01512225

Enhancing Breast Milk Production With Domperidone in Mothers of Preterm Neonates

The purpose of this study is to evaluate the safety and efficacy of Domperidone in those mothers who are identified as having difficulty with breast milk production to meet the nutritional needs of their infant in the neonatal intensive are unit hospitalization setting, and to determine how it should be considered in the care of mothers and their preterm infants without causing undesirable effects to either the mother or infant.

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Key information

Age range

18 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

Sunnybrook Health Sciences Centre

Toronto, Ontario, M4N 3M5, Canada

About this study

It is widely acknowledged that recent perinatal and neonatal technological advances (eg. assisted ventilation, surfactant, antenatal corticosteroids) have greatly enhanced the survival rate of very low birth weight and extremely low birth weight infants. A compelling body of evidence now exists to suggest that use of breast milk to feed preterm infants during initial hospitalization positively impacts their neurodevelopment during early childhood and beyond. In order to provide breastmilk, mothers of preterm infants have to begin to produce and mechanically express milk. However, these mothers are often faced with challenges in maintaining an adequate volume that will meet their infants' nutritional needs, as well as declines in production after several weeks despite a myriad of measures designed to assist in production. The primary hypothesis for this study is that Domperidone, through its pharmacologic action on increasing prolactin levels, will assist mothers experiencing inadequate breast milk production in increasing breast milk volumes to a level identified as being sufficient for continued pumping in the hospitalization period.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • mothers of a preterm infant born < 30 completed weeks gestation (23 0/7-29 6/7 weeks)
  • postpartum period of 7-21 days
  • mechanically pumping a minimum average of 6 times a day in the 4-7 days prior to enrollment
  • experiencing inadequate milk supply defined as providing < 100% of the average of the daily nutritional intake during the previous 72-hour period prior to enrollment based on a fluid intake of 250 mL/kg/d or experiencing a clinical reduction of approximately 20% from a peak volume during the previous 72-hour period prior to enrollment

Exclusion criteria

  • history of known or suspected cardiac dysrhythmias (tachyarrhythmia, Q-Tc prolongation) or currently on an anti-arrhythmic medication
  • currently experiencing mastitis
  • previous breast surgery, including augmentation or reduction, nipple piercing and/or the use of nipple rings/studs within the last year, or any reduction
  • known chronic or debilitating illness, known abnormal liver function or gastric abnormalities gastrointestinal that will be exacerbated by the use of a prokinetic, examples include hemorrhage or blockage, actively treated with acid reflux which requires treatment for greater than 5 days and includes H2 blockers (occasional use of H2 blockers for heartburn or mild acid reflux is not considered an exclusion) and HIV
  • known to have a prolactin-releasing pituitary tumor
  • receiving medications known to alter the metabolism and pharmacokinetics of domperidone (eg. oral "azole" antifungals, erythromycin antibiotics, monoamine oxidase inhibitors (MAO) inhibitors) or medications that have dopaminergic or antidopaminergic activity or affect prolactin levels
  • mothers of higher order pregnancies (triplet, or more)
  • currently smoking 6 or more cigarette per day as reported by the mother

Treatment and study plan

Domperidone maleate

Drug

domperidone maleate tablet 10 mg orally three times daily for 28 days

Placebo Tablet

Drug

placebo tablet 10 mg orally three times daily for 14 days

Primary outcomes

  1. Increase in Breast Milk Production

    Time frame: Day 0 to day 14

    The primary outcome is the difference in the proportion of women having a 50% increase in breast milk volume at the end of 14 days of treatment with domperidone compared to mothers receiving placebo (mean day 14 volume minus mean day 0 volume at entry).

Secondary outcomes

  1. Increase in Breast Milk Volume on Day 28

    Time frame: day 0 to day 28

    Number of mothers who achieved 50% increase in milk volume on day 28

  2. Mean Breast Milk Volumes on Day 14

    Time frame: Day 0 and day 14

    Mean milk volumes between the two groups at 14 days of study intervention

  3. Mean Breast Milk Volumes on Day 28

    Time frame: day 0 and 28

    Mean milk volumes between the two groups at 28 days of study intervention

  4. Mean Volume Change From Day 0 to Day 14

    Time frame: days 0 and 14

    change on the volume of milk from day 0 to day 14 between the two groups

  5. Mean Volume Change on the Volume of Milk From Day 15 to Day 28

    Time frame: day 15 and day 28

    change on the volume of milk from day 15 to day 28 between the two groups

  6. Provision of Breast Milk at Term Gestation

    Time frame: term gestation

    provision of breast milk as the primary source of nutrition

  7. Provision of Breast Milk at 6 Weeks Post Term Gestation

    Time frame: 6 weeks post term gestation

    Provision of breast milk at 6 weeks post term gestation as primary source of nutrition

Sponsors and collaborators

Lead sponsor

Sunnybrook Health Sciences Centre

Other

Registry information

Acronym: EMPOWER

Important dates

Study start
2012
Primary completion
2015
Study completion
2016
First posted
Jan 19, 2012
Registry last updated
Apr 20, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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