Phase 2
N=90
Enhancing Breast Milk Production With Domperidone in Mothers of Preterm Neonates
Low Milk Supply
Bottom Line
View on ClinicalTrials.gov: NCT01512225 ↗Enrolled (actual)
90
Serious AEs
0.0%
Results posted
Apr 2017
Primary outcome: Primary: Increase in Breast Milk Production — 35; 26 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- Domperidone maleate (Drug); Placebo Tablet (Drug)
- Age
- Adult · 18+ yrs
- Sex
- Female
- Sponsor
- Sunnybrook Health Sciences Centre
- Primary completion
- Oct 2015
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Increase in Breast Milk Production |
35; 26 | — |
| SECONDARY Increase in Breast Milk Volume on Day 28 |
31; 28 | — |
| SECONDARY Mean Breast Milk Volumes on Day 14 |
267; 217 | — |
| SECONDARY Mean Breast Milk Volumes on Day 28 |
290; 302 | — |
| SECONDARY Mean Volume Change From Day 0 to Day 14 |
254; 175 | — |
| SECONDARY Mean Volume Change on the Volume of Milk From Day 15 to Day 28 |
22; 49 | — |
| SECONDARY Provision of Breast Milk at Term Gestation |
26; 27 | — |
| SECONDARY Provision of Breast Milk at 6 Weeks Post Term Gestation |
19; 20 | — |
Summary
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.
Eligibility Criteria
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
Data sourced from ClinicalTrials.gov (NCT01512225). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.