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To Determine the Best Feeding Practice in Preterm Infants on Non-invasive Ventilation.

Primary Purpose

Prematurity; Extreme, Feeding Patterns, Ventilator Lung; Newborn

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Continuous Feeds
Intermittent Bolus Feeds
Sponsored by
Rajeev Kumar
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Prematurity; Extreme focused on measuring Preterm infants, Feeding methods, bolus feeds, continuous feeds, non-invasive ventilation, RAM cannula

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Preterm Infants 24- 34 weeks of gestation On Non-invasive ventilation (NIPPV/CPAP/HFNC) Nothing by mouth (NPO) or on trophic feeds (<20 ml/kg/day) at the time of randomization. Exclusion Criteria: Gestational Age > 34 weeks Infants on invasive ventilation or low flow nasal cannula and on feeding volume more than trophic feeds. Major congenital anomalies.

Sites / Locations

  • Cook County HelathRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Bolus Feeding

Continuous Feeding

Arm Description

Intermittent bolus feeding will be defined as delivering enteral nutrition multiple times, usually every 2-3 hours over 15 - 30 minutes by gravity or an electric pump. It will be further stratified as per weight ( less than 1000 g, 1000-1500 g, >1500 g).

Continuous feeding will be defined as delivering enteral nutrition with constant speed for 24 hours via a nutritional pump. It will be further stratified as per weight ( less than 1000 g, 1000-1500 g, >1500 g).

Outcomes

Primary Outcome Measures

Day of life to reach full feeds
the day of life to reach full feed, that is, 120 ml/kg/day.

Secondary Outcome Measures

Feeding interruptions
Interruptions while feeding, which includes NPO days, Lab usage and Radiological evaluation.
Time to reach (day of life) first oral feed
Day of life when infant was taking oral feeds (no feeds by nasogastric tube)
Weight gain, head circumference (HC) and Length.
Anthropometric parameters
Length of hospital stay
Total duration of hospital stay
Use of investigative medicine for feeding intolerance
Use of radiographic imaging or blood work-up to rule out any feeding intolerance

Full Information

First Posted
March 28, 2023
Last Updated
August 29, 2023
Sponsor
Rajeev Kumar
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1. Study Identification

Unique Protocol Identification Number
NCT05824377
Brief Title
To Determine the Best Feeding Practice in Preterm Infants on Non-invasive Ventilation.
Official Title
To Determine the Best Feeding Practice in Preterm Infants on Non-invasive Ventilation.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 1, 2023 (Actual)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
February 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Rajeev Kumar

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To evaluate the duration to reach full feeds by comparing continuous gavage feeds versus bolus feeds in preterm infants who are on non-invasive respiratory support (RAM cannula - short binasal prongs).
Detailed Description
Methods: The study will be a randomized control trial at our NICU (Neonatal Intensive Care Unit) (Level III). Preterm infants on non -invasive ventilation (nasal intermittent positive pressure ventilation (NIPPV)/ continuous positive airway pressure (CPAP)) will be randomly assigned into either continuous feeds or bolus feeds groups. Baby will be fed enterally through a nasogastric tube via continuous or bolus feeds using either maternal milk or formula, according to parental choice. Feeds will be advanced as per the feeding guidelines or per treating physician. Currently we use both bolus and continuous feeding practice in our NICU, as per physician's discretion. Intervention: Infants will be randomized into 2 groups; one will receive continuous nasogastric feeding and the other group will receive intermittent bolus feeds. Continuous feeds will be delivered via an indwelling nasogastric/orogastric tube with a continuous infusion pump. Intermittent bolus feedings will be given by gravity every 3 hours over 15- 30 minutes. Parents' consent will be taken when the infant is qualified for the study. The consent will be taken by one of the coinvestigators. Each coinvestigator will be trained to consent for standardization. Non-English-speaking parents will be consented using the medical video interpreter (Voyce). Accent will not be obtained as neonates aren't mature to give accent. Patients will be randomized into each group by pulling a sealed envelope. Monitoring for complications: During the study, infants will be monitored for any complications due to either feeding protocol like feeding intolerance, reflux, abdominal distension, poor weight gain, any risk of aspiration pneumonia or necrotizing enterocolitis (NEC). Such symptoms are usually monitored by our NICU team as per our guidelines. These feeding issues can be encountered in either group. If such problems are encountered, feeding protocol will be changed as per the physician's clinical decision. Parents will be informed of the changes. Intention to treat protocol will be used while calculating the statistical analysis. Guidelines for withholding the feeds (bolus or intermittent) or changing either group will be: Excessive gastric residual (> 50% of the volume fed) Increase in abdominal girth (>1.5-2.5 cm along with other signs and symptoms of intolerance to feeds) Poor/slow weight gain (rate of weight gain is significantly below that expected for age and sex, or if weight has dropped ≥2 major percentile lines) Occult blood positive in stools/visible blood in the stools Concerns for neonatal sepsis clinically as per attending's discretion Apnea pertaining for more than 20 secs alone or apnea for > 10 seconds along with bradycardia (<80) or desaturations (hypoxemia as per gestational age); and occurring more than 2 or 3 times a day and requiring intervention Abnormal Abdominal X rays concerning for suspected NEC or NEC as per Bell's criteria Infants who need to be on invasive ventilation Treating physician's clinical decision Feeding protocol: BW: 500 -1000 grams: Initiate: When baby is stable. Start with trophic feeds, that is, 5 -10 ml/kg/day. Advance: If tolerating trophic feeds for 2-3 days, advance feeds by 10 ml/kg/day. Initial choice of milk: Breast Milk/Donor Breast Milk / Formula (Enfamil) - 20Kcal/Oz. Fortify: When 60-80 ml/kg/day feeds are reached, fortify to 22Kcal/Oz and within next few days to 24 Kcal/Oz. BW 1000 - 1500 grams: Initiate: When baby is stable. Trophic feeds 5-10 ml/kg/day. Advance: 15-20 ml/kg/day Initial choice of milk, fortifying and full feeds as above. BW 1500 grams and above: Initiate: 30 ml/kg/day. Advance: 20 -35 ml/kg/day Initial choice of milk, fortifying and full feeds as above.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prematurity; Extreme, Feeding Patterns, Ventilator Lung; Newborn
Keywords
Preterm infants, Feeding methods, bolus feeds, continuous feeds, non-invasive ventilation, RAM cannula

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Infants will be randomized into 2 groups; one will receive continuous nasogastric feeding and the other group will receive intermittent bolus feeds. Each group will be stratified as per weight, thus (<1000 g, 1000-1500 g, and > 1500 g). It will be 1-1 randomization and will be randomized into each group by pulling a sealed envelope. Protected Health Information (PHI) will be de-identified by assigning a study code. Sample size: A sample size of at least 23 in each arm was calculated using the SAS system. A power of 80% and a mean difference of 40% decrease in the length of time to achieve full feeds; and an SD of 8.5 was considered while calculating the number of patients. The mean length of time to achieve full feeds in our NICU as per chart review was 17 +/- 8.5 days.
Masking
Outcomes Assessor
Masking Description
Caregivers, study personnel and nurses will not be blinded, as blinding will be hard for the treating team. Parents will not be blinded as we inform about the infant's progress and plan routinely. Statisticians will be blinded during (they will receive de-identified data).
Allocation
Randomized
Enrollment
46 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Bolus Feeding
Arm Type
Experimental
Arm Description
Intermittent bolus feeding will be defined as delivering enteral nutrition multiple times, usually every 2-3 hours over 15 - 30 minutes by gravity or an electric pump. It will be further stratified as per weight ( less than 1000 g, 1000-1500 g, >1500 g).
Arm Title
Continuous Feeding
Arm Type
Experimental
Arm Description
Continuous feeding will be defined as delivering enteral nutrition with constant speed for 24 hours via a nutritional pump. It will be further stratified as per weight ( less than 1000 g, 1000-1500 g, >1500 g).
Intervention Type
Other
Intervention Name(s)
Continuous Feeds
Intervention Description
Continuous feeds will be delivered via an indwelling nasogastric/orogastric tube with a continuous infusion pump.
Intervention Type
Other
Intervention Name(s)
Intermittent Bolus Feeds
Intervention Description
Intermittent bolus feedings will be given by gravity every 3 hours over 15- 30 minutes.
Primary Outcome Measure Information:
Title
Day of life to reach full feeds
Description
the day of life to reach full feed, that is, 120 ml/kg/day.
Time Frame
From the date of randomization until the date of NICU discharge/death, assessed up to 1 year.
Secondary Outcome Measure Information:
Title
Feeding interruptions
Description
Interruptions while feeding, which includes NPO days, Lab usage and Radiological evaluation.
Time Frame
From the date of randomization until the date of NICU discharge/death, assessed up to 1 year.
Title
Time to reach (day of life) first oral feed
Description
Day of life when infant was taking oral feeds (no feeds by nasogastric tube)
Time Frame
From the date of randomization until the date of NICU discharge/death, assessed up to 1 year.
Title
Weight gain, head circumference (HC) and Length.
Description
Anthropometric parameters
Time Frame
From the date of randomization until the date of NICU discharge/death, assessed up to 1 year.
Title
Length of hospital stay
Description
Total duration of hospital stay
Time Frame
From the date of randomization until the date of NICU discharge/death, assessed up to 1 year.
Title
Use of investigative medicine for feeding intolerance
Description
Use of radiographic imaging or blood work-up to rule out any feeding intolerance
Time Frame
From the date of randomization until the date of NICU discharge/death, assessed up to 1 year.

10. Eligibility

Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Preterm Infants 24- 34 weeks of gestation On Non-invasive ventilation (NIPPV/CPAP/HFNC) Nothing by mouth (NPO) or on trophic feeds (<20 ml/kg/day) at the time of randomization. Exclusion Criteria: Gestational Age > 34 weeks Infants on invasive ventilation or low flow nasal cannula and on feeding volume more than trophic feeds. Major congenital anomalies.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Aashika Janwadkar, MD
Phone
6469343483
Email
aashika.janwadkar@cookcountyhealth.org
First Name & Middle Initial & Last Name or Official Title & Degree
Rajeev Kumar, MD
Phone
6308652091
Email
rkumar3@cookcountyhhs.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rajeev Kumar, MD
Organizational Affiliation
Cook County Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cook County Helath
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rajeev Kumar, MD
First Name & Middle Initial & Last Name & Degree
Rajeev Kumar, MD
First Name & Middle Initial & Last Name & Degree
Aashika Janwadkar, MD
First Name & Middle Initial & Last Name & Degree
Aarti Kulkarni, MD
First Name & Middle Initial & Last Name & Degree
Nita Shrestha, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30658676
Citation
Cresi F, Maggiora E, Borgione SM, Spada E, Coscia A, Bertino E, Meneghin F, Corvaglia LT, Ventura ML, Lista G; ENTARES Study Research Group. Enteral Nutrition Tolerance And REspiratory Support (ENTARES) Study in preterm infants: study protocol for a randomized controlled trial. Trials. 2019 Jan 18;20(1):67. doi: 10.1186/s13063-018-3119-0.
Results Reference
background
PubMed Identifier
31659243
Citation
Wang Y, Zhu W, Luo BR. Continuous feeding versus intermittent bolus feeding for premature infants with low birth weight: a meta-analysis of randomized controlled trials. Eur J Clin Nutr. 2020 May;74(5):775-783. doi: 10.1038/s41430-019-0522-x. Epub 2019 Oct 28.
Results Reference
background
PubMed Identifier
34091605
Citation
Mukerji A, Abdul Wahab MG, Razak A, Rempel E, Patel W, Mondal T, Beck J. High CPAP vs. NIPPV in preterm neonates - A physiological cross-over study. J Perinatol. 2021 Jul;41(7):1690-1696. doi: 10.1038/s41372-021-01122-6. Epub 2021 Jun 5.
Results Reference
background
PubMed Identifier
22071802
Citation
Premji SS, Chessell L. Continuous nasogastric milk feeding versus intermittent bolus milk feeding for premature infants less than 1500 grams. Cochrane Database Syst Rev. 2011 Nov 9;2011(11):CD001819. doi: 10.1002/14651858.CD001819.pub2.
Results Reference
background
PubMed Identifier
32086439
Citation
Dumpa V, Kamity R, Ferrara L, Akerman M, Hanna N. The effects of oral feeding while on nasal continuous positive airway pressure (NCPAP) in preterm infants. J Perinatol. 2020 Jun;40(6):909-915. doi: 10.1038/s41372-020-0632-2. Epub 2020 Feb 21.
Results Reference
background
PubMed Identifier
9310537
Citation
Akintorin SM, Kamat M, Pildes RS, Kling P, Andes S, Hill J, Pyati S. A prospective randomized trial of feeding methods in very low birth weight infants. Pediatrics. 1997 Oct;100(4):E4. doi: 10.1542/peds.100.4.e4.
Results Reference
background

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To Determine the Best Feeding Practice in Preterm Infants on Non-invasive Ventilation.

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