Feeding; Difficult, Newborn Clinical Trial
Official title:
Randomized Crossover Trial of the Nifty Feeding Cup and a Medicine Cup in Preterm Infants Who Have Difficulty Breastfeeding
Verified date | August 2019 |
Source | PATH |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The investigators will establish an evidence base for the Nifty Feeding Cup by evaluating its effectiveness and caregiver satisfaction. The investigators will conduct a randomized crossover trial that compares the Nifty Feeding Cup to a standardized, generic medicine cup used to feed preterm infants with breastfeeding difficulties at Komfo Anokye Teaching Hospital (KATH) in Kumasi, Ghana.
Status | Completed |
Enrollment | 200 |
Est. completion date | September 25, 2018 |
Est. primary completion date | September 25, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: Infant - Born preterm (<37 weeks gestational age) at time of birth - Corrected gestational age is <37 weeks per the modified Dubowitz score on date of enrollment - Diagnosed with feeding difficulties - Patient in the mother-baby unit at KATH - Clinically indicated to start cup feeding (including an infant who has a nasogastric tube and is cup feeding or indicated to start cup feeding) - Has an anticipated hospital stay that is at least 48 hours Caregiver: - At least 18 years of age - One of the following biologic family members of the infant (Mother, Grandmother, Aunt) - Self-identifies as the primary feeder of the infant - Prior experience feeding the potential infant participant with nipple feeding (e.g. breast feeding, bottle feeding) or nasogastric [NG] tube - Verifies willingness to comply with all study procedures Exclusion Criteria: Infant - Congenital anomaly except for minor anomalies (e.g. an extra digit or ear tag is okay) - Other condition or situation that makes infant unlikely to be able to comply with study procedures. Examples include the infant anticipated to not be in hospital long enough, infant has a suspected intestinal obstruction, or necrotizing enterocolitis. - No mother, grandmother, or aunt caregiver available to participate in study - Enrolled in another study at KATH that would interfere with his/her ability to participate in this study. |
Country | Name | City | State |
---|---|---|---|
Ghana | Komfo Anokye Teaching Hospital (KATH) | Kumasi |
Lead Sponsor | Collaborator |
---|---|
PATH | Komfo Anokye Teaching Hospital, Seattle Children's Hospital |
Ghana,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Caregiver Satisfaction [Immediate] | Caregiver's satisfaction will be the cup she prefers, which will be recorded in the In-Hospital Preference Survey completed after the caregiver has finished the feeding portion of the study. Data refers to number of caregivers who prefer the Nifty Cup. | 24-36 hours | |
Primary | Spillage | Spillage will be reported as a percent with the amount of milk in grams spilled/mopped up divided by the total amount of milk weighed in grams less the total amount of milk not used. Each caregiver-infant pair will be provided with a bib cloth for each observed feeding. The bib cloth will be weighed before and after each feed and the weights recorded on the Feeding Assessment form. The difference between the pre and post weights will be used as the measure of the amount spilled. A digital scale will be used to measure the milk weight, which will be recorded in grams. | 24-36 hours |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03445689 -
Oxygenation Instability and Maturation of Control of Breathing in Premature Infants
|
||
Completed |
NCT03245723 -
Cardiac Function and Metabolism in Young Adults Born Premature (PET-MRI)
|
N/A | |
Active, not recruiting |
NCT03575897 -
Serial Assessment of Body Fat Accrual in Very Preterm Infants
|
N/A | |
Completed |
NCT03082313 -
Movement-based Infant Intervention
|
N/A | |
Completed |
NCT03696758 -
Improving Right Ventricular Function in Young Adults Born Preterm
|
Phase 2 | |
Withdrawn |
NCT01569633 -
Use of Prokinetics in Early Enteral Feeding in Preterm Infants
|
N/A | |
Terminated |
NCT03532555 -
Enteral Zinc to Improve Growth in Infants at Risk for Bronchopulmonary Dysplasia
|
N/A | |
Completed |
NCT03230032 -
Pacifier Activated Device and Mother's Voice in Infants at High-risk for Cerebral Palsy
|
N/A | |
Recruiting |
NCT03693287 -
Personalized vs Standardized PN for Preterm Infants >1250g
|
Phase 4 | |
Terminated |
NCT03542812 -
L-citrulline and Pulmonary Hypertension Associated With Bronchopulmonary Dysplasia
|
Early Phase 1 | |
Completed |
NCT03434743 -
Non-nutritive Sucking and Breastfeeding in Preterm Infants
|
N/A | |
Active, not recruiting |
NCT03168516 -
Effects of Closed-loop Automatic Control of FiO2 in Extremely Preterm Infants
|
Phase 3 | |
Completed |
NCT03357458 -
Parent-child Interactions, Child Developmental Health, and Health System Costs at 6 Months Corrected Age
|
N/A | |
Recruiting |
NCT03521063 -
Efficacy of Adding Budesonide to Poractant Alfa to Prevent Bronchopulmonary Dysplasia.
|
Phase 4 | |
Recruiting |
NCT03501485 -
Impact of Protein Supplementation to Mother Milk on Resting Energy Expenditure (REE) in Growing Healthy Preterm Infants.
|
||
Recruiting |
NCT06416956 -
Baby-CINO: CaffeINe Treatment Optimisation in Premature Infants
|
||
Completed |
NCT03586856 -
Comparison of Leakage With Nasal Prongs and Nasal Mask Interface in Newborns Receiving CPAP Treatment
|
N/A | |
Completed |
NCT03333161 -
Prematurity Related Ventilatory Control (PRE-VENT) - Specific Aim 2
|
N/A | |
Completed |
NCT03333174 -
Prematurity Related Ventilatory Control (PRE-VENT) - Specific Aim 3
|
N/A | |
Active, not recruiting |
NCT03558737 -
Nasal High-frequency Jet Ventilation (nHFJV) Following Extubation in Preterm Infants
|
N/A |