search
Back to results

Duodenal Feeds in Very Low Birth Weight Infants

Primary Purpose

BPD - Bronchopulmonary Dysplasia, VLBW - Very Low Birth Weight Infant, Feeding Disorder Neonatal

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Mode of Delivery of Feeds
Sponsored by
Johns Hopkins All Children's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for BPD - Bronchopulmonary Dysplasia focused on measuring Duodenal feeds, Transpyloric feeds, Bronchopulmonary Dysplasia, BPD, Premature infant, Neonate

Eligibility Criteria

0 Days - 12 Months (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Infants admitted to the Johns Hopkins All Children's NICU before 72 hours of life
  • Infants with a birth weight <1251g

Exclusion Criteria:

  • First obtained pH <7.0
  • APGAR <5 at 5 minutes (The Apgar score is a test given to newborns soon after birth. This test checks a baby's heart rate, muscle tone, and other signs to see if extra medical care or emergency care is needed. Appearance, Pulse, Grimace, Activity, Respiration (APGAR))
  • Infants on hydrocortisone for hypotension prior to randomization
  • Infants with intrauterine growth restriction (IUGR) defined by birth weight ≤10th percentile for gestational age
  • Infants with congenital anomalies, including but not limited to: Chromosomal abnormalities;Structural airway or pulmonary abnormalities (e.g. tracheoesophageal fistulas, cleft palate, congenital pulmonary adenomatous malformation, etc.); Abdominal anomalies requiring surgical interventions (e.g. intestinal atresia, intestinal webs, gastroschisis, omphalocele, anal atresia); Major cardiac anomalies
  • Infants with a history of intestinal perforation or NEC
  • Presence of gastrostomy tube
  • Infants who have not been initiated on any volume of enteral feeds by 10 days of life

Sites / Locations

  • Johns Hopkins All Children's HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Gastric Feeds

Duodenal Feeds

Arm Description

Patients in this arm will receive feeds via the standard route which is gastric feeds.

Patients in this arm will receive feeds via the experimental route which is duodenal feeds.

Outcomes

Primary Outcome Measures

Number of successful placements of duodenal tubes
Success to be measured by appropriate placement of the duodenal tube within the duodenum as confirmed by radiographic imaging.
Safety as assessed by number of intestinal perforations
Safety of duodenal feeds in very low birth weight infants as measured by the number of intestinal perforations secondary to placement of duodenal tube.

Secondary Outcome Measures

Supplemental oxygen requirement
Number of days on supplemental oxygen >21% throughout duration of hospitalization
Number of participants with Bronchopulmonary Dysplasia
Mild, moderate, severe Bronchopulmonary Dysplasia (BPD) as defined by the NICHD/NHLBI/ORD Workshop published in 2001
Number of deaths during hospitalization
Number of days of mechanical ventilation
Days of invasive mechanical ventilation up until hospital discharge
Number of participants with late-onset sepsis
Number of participants diagnosed with Culture-positive sepsis after 72 hours of life
Central line days
Cumulative days of indwelling central venous catheters (peripherally inserted central catheters, tunneled venous catheters, umbilical venous catheters)
Number of participants with necrotizing enterocolitis
Number of participants with necrotizing enterocolitis (NEC) defined by Modified Bells Stage II or greater
Number of replaced enteral tubes
Number of replaced enteral tubes, gastric or duodenal, per patient
Number of Radiographs related to enteral tube placement
Number of radiographs obtained with the indication of enteral tube placement, gastric or duodenal
Weight percentile at 36 weeks postmenstrual age
Weight percentile at 36 weeks postmenstrual age
Height percentile at 36 weeks postmenstrual age
Height percentile at 36 weeks postmenstrual age
Head circumference percentile at 36 weeks postmenstrual age
Head circumference percentile at 36 weeks postmenstrual age
Z-scores for weight at 36 weeks postmenstrual age
Z-scores for weight at 36 weeks postmenstrual age calculated using PediTools
Z-scores for height at 36 weeks postmenstrual age
Z-scores for height at 36 weeks postmenstrual age calculated using PediTools
Z-scores for head circumference at 36 weeks postmenstrual age
Z-scores for head circumference at 36 weeks postmenstrual age calculated using PediTools
Daily daily weight gain
Average daily weight gain (kg/day) calculated from birth until 36 weeks postmenstrual age using the fetal-infant growth reference (FIGR) equation
Length of stay
Length of hospital stay (days)
Need for excess fortification of feeds
Number of participants requiring fortification beyond 24kcal/oz
Use of postnatal dexamethasone
Number of participants requiring use of postnatal dexamethasone for respiratory indications
Use of chronic diuretics
Number of participants requiring use of chronic diuretics including thiazide diuretics and spironolactone

Full Information

First Posted
January 22, 2020
Last Updated
June 22, 2023
Sponsor
Johns Hopkins All Children's Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT04246333
Brief Title
Duodenal Feeds in Very Low Birth Weight Infants
Official Title
Feasibility and Safety of Duodenal Feeds in Very Low Birth Weight Infants
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 7, 2020 (Actual)
Primary Completion Date
June 30, 2024 (Anticipated)
Study Completion Date
October 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins All Children's Hospital

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
Premature infants have high rates of bronchopulmonary dysplasia (BPD) due to prematurity of the participants' lungs and the need for prolonged respiratory support. These infants are at increased risk for gastroesophageal reflux and aspiration which may exacerbate lung injury. Transpyloric feeds, specifically duodenal feeds, may be used to bypass the stomach and directly feed the duodenum decreasing the amount of gastric reflux contributing to aspiration. Duodenal feeds are equivalent to gastric feeds with regards to nutritional outcomes, and have been shown to decrease events of apnea and bradycardia in premature infants. This study will evaluate the feasibility and safety of duodenal feeds in premature infants. The hypothesis is that duodenal feeds may be safely and successfully performed in premature very low birth weight infants.
Detailed Description
The primary outcome of this study is the safety and feasibility of duodenal feeds in very low birth weight infants. The secondary outcomes are various measures related to growth, respiratory support, comorbidities, and hospitalization. Eligibility of infants admitted to the Johns Hopkins All Children's Neonatal Intensive Care Unit (NICU) will be determined based on inclusion and exclusion criteria. Eligible infants will be recruited and enrolled by 14 days of life after informed consent is obtained. Randomization of the infants into two groups- investigational continuous Duodenal Feeds (DF) or standard Gastric Feeds (GF) - will occur just prior to the infants advancing beyond 50mL/kg/day of enteral feeds. All enrolled infants will be fed per the institutional feeding protocol. Once infants advance past 50mL/kg/day of enteral feeds, at this point infants will be randomized to DF or GF groups in a 1:1 block randomization using blinded envelopes. Multiple gestation infants will be randomized individually. Placement of gastric tubes will be per standard of practice, and insertion of duodenal tube will be per manual of operations. Continuous duodenal feeds will be provided over 24 hours as a continuous infusion through a nasoduodenal or oro-duodenal tube. Standard gastric feeds will be infused via a nasogastric or orogastric tube per the instructions of the medical team. Gastric feeds are provided as standard of care in the NICU; intermittent bolus feeds over 15-60 minutes. Feeding time may be prolonged by the medical team, for longer than 60 minutes and possibly even be given continuously, for various reasons (emesis, reflux, apnea, bradycardia, etc.) and will be monitored and recorded. Feed volume and advancement will continue to be determined by standardized institutional feeding guidelines. Decision to provide further fortification of feeds beyond institutional guidelines will be determined by the medical team and not standardized in this protocol. Once full enteral feeds are achieved (total fluid goal of at least 140mL/kg/day), patients will continue to receive feeds via the designated route. An institutional "Infant Driven Feeding Guideline" is utilized to evaluate readiness to orally feed and to transition premature infants from enteral to oral feeds. Once an infant is eligible to receive oral feeds per this guideline (32 weeks postmenstrual age, and tolerating ≤2L flow via nasal cannula for at least 24 hours), the study will allow the medical team to transition infants in the DF group to gastric feeds. Regarding transitioning infant from duodenal to gastric feeds, infants are initially placed on continuous gastric feeds, and once the participants have demonstrated tolerance (no evidence of reflux, increased respiratory support, emesis), the participants are then transitioned to bolus gastric feeds progressively. Infants may be allowed to orally feed during this transition period if the participants meet the appropriate infant driven feeding scores per protocol. All infants in this study will be monitored for primary and secondary outcomes through the duration of admission and up until the time of discharge. Safety events will be frequently monitored for throughout the duration of admission and addressed immediately if warranted.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
BPD - Bronchopulmonary Dysplasia, VLBW - Very Low Birth Weight Infant, Feeding Disorder Neonatal, Feeding; Difficult, Newborn, Premature Birth, Chronic Lung Disease of Prematurity
Keywords
Duodenal feeds, Transpyloric feeds, Bronchopulmonary Dysplasia, BPD, Premature infant, Neonate

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Gastric Feeds
Arm Type
No Intervention
Arm Description
Patients in this arm will receive feeds via the standard route which is gastric feeds.
Arm Title
Duodenal Feeds
Arm Type
Experimental
Arm Description
Patients in this arm will receive feeds via the experimental route which is duodenal feeds.
Intervention Type
Other
Intervention Name(s)
Mode of Delivery of Feeds
Intervention Description
Eligible infants will be recruited and enrolled and randomized to either duodenal feeds (DF) or gastric feeds (GF), which will occur just prior to the infants advancing beyond 50mL/kg/day of enteral feeds. All enrolled infants will be fed per our institutional feeding protocol. Once infants advance past a volume of 50mL/kg/day of enteral feeds, at this point infants will be randomized to DF or GF groups.
Primary Outcome Measure Information:
Title
Number of successful placements of duodenal tubes
Description
Success to be measured by appropriate placement of the duodenal tube within the duodenum as confirmed by radiographic imaging.
Time Frame
12 months
Title
Safety as assessed by number of intestinal perforations
Description
Safety of duodenal feeds in very low birth weight infants as measured by the number of intestinal perforations secondary to placement of duodenal tube.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Supplemental oxygen requirement
Description
Number of days on supplemental oxygen >21% throughout duration of hospitalization
Time Frame
duration of hospitalization, up to 15 months
Title
Number of participants with Bronchopulmonary Dysplasia
Description
Mild, moderate, severe Bronchopulmonary Dysplasia (BPD) as defined by the NICHD/NHLBI/ORD Workshop published in 2001
Time Frame
15 months
Title
Number of deaths during hospitalization
Time Frame
15 months
Title
Number of days of mechanical ventilation
Description
Days of invasive mechanical ventilation up until hospital discharge
Time Frame
15 months
Title
Number of participants with late-onset sepsis
Description
Number of participants diagnosed with Culture-positive sepsis after 72 hours of life
Time Frame
15 months
Title
Central line days
Description
Cumulative days of indwelling central venous catheters (peripherally inserted central catheters, tunneled venous catheters, umbilical venous catheters)
Time Frame
15 months
Title
Number of participants with necrotizing enterocolitis
Description
Number of participants with necrotizing enterocolitis (NEC) defined by Modified Bells Stage II or greater
Time Frame
15 months
Title
Number of replaced enteral tubes
Description
Number of replaced enteral tubes, gastric or duodenal, per patient
Time Frame
15 months
Title
Number of Radiographs related to enteral tube placement
Description
Number of radiographs obtained with the indication of enteral tube placement, gastric or duodenal
Time Frame
15 months
Title
Weight percentile at 36 weeks postmenstrual age
Description
Weight percentile at 36 weeks postmenstrual age
Time Frame
At 36 weeks
Title
Height percentile at 36 weeks postmenstrual age
Description
Height percentile at 36 weeks postmenstrual age
Time Frame
At 36 weeks
Title
Head circumference percentile at 36 weeks postmenstrual age
Description
Head circumference percentile at 36 weeks postmenstrual age
Time Frame
At 36 weeks
Title
Z-scores for weight at 36 weeks postmenstrual age
Description
Z-scores for weight at 36 weeks postmenstrual age calculated using PediTools
Time Frame
At 36 weeks
Title
Z-scores for height at 36 weeks postmenstrual age
Description
Z-scores for height at 36 weeks postmenstrual age calculated using PediTools
Time Frame
At 36 weeks
Title
Z-scores for head circumference at 36 weeks postmenstrual age
Description
Z-scores for head circumference at 36 weeks postmenstrual age calculated using PediTools
Time Frame
At 36 weeks
Title
Daily daily weight gain
Description
Average daily weight gain (kg/day) calculated from birth until 36 weeks postmenstrual age using the fetal-infant growth reference (FIGR) equation
Time Frame
At 36 weeks
Title
Length of stay
Description
Length of hospital stay (days)
Time Frame
duration of hospitalization, up to 15 months
Title
Need for excess fortification of feeds
Description
Number of participants requiring fortification beyond 24kcal/oz
Time Frame
15 months
Title
Use of postnatal dexamethasone
Description
Number of participants requiring use of postnatal dexamethasone for respiratory indications
Time Frame
15 months
Title
Use of chronic diuretics
Description
Number of participants requiring use of chronic diuretics including thiazide diuretics and spironolactone
Time Frame
15 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
0 Days
Maximum Age & Unit of Time
12 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Infants admitted to the Johns Hopkins All Children's NICU before 72 hours of life Infants with a birth weight <1251g Exclusion Criteria: First obtained pH <7.0 APGAR <5 at 5 minutes (The Apgar score is a test given to newborns soon after birth. This test checks a baby's heart rate, muscle tone, and other signs to see if extra medical care or emergency care is needed. Appearance, Pulse, Grimace, Activity, Respiration (APGAR)) Infants on hydrocortisone for hypotension prior to randomization Infants with intrauterine growth restriction (IUGR) defined by birth weight ≤10th percentile for gestational age Infants with congenital anomalies, including but not limited to: Chromosomal abnormalities;Structural airway or pulmonary abnormalities (e.g. tracheoesophageal fistulas, cleft palate, congenital pulmonary adenomatous malformation, etc.); Abdominal anomalies requiring surgical interventions (e.g. intestinal atresia, intestinal webs, gastroschisis, omphalocele, anal atresia); Major cardiac anomalies Infants with a history of intestinal perforation or NEC Presence of gastrostomy tube Infants who have not been initiated on any volume of enteral feeds by 10 days of life
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Prem Fort, MD
Phone
727-767-4313
Email
pfort1@jh.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Noura Nickel, MD
Phone
727-767-4313
Email
nnickel1@jh.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Prem Fort, MD
Organizational Affiliation
Johns Hopkins All Children's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins All Children's Hospital
City
Saint Petersburg
State/Province
Florida
ZIP/Postal Code
33701
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Noura Nickel
Phone
502-439-4120
Email
noura.nickel@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
11401896
Citation
Jobe AH, Bancalari E. Bronchopulmonary dysplasia. Am J Respir Crit Care Med. 2001 Jun;163(7):1723-9. doi: 10.1164/ajrccm.163.7.2011060. No abstract available.
Results Reference
background
PubMed Identifier
23758808
Citation
Fenton TR, Nasser R, Eliasziw M, Kim JH, Bilan D, Sauve R. Validating the weight gain of preterm infants between the reference growth curve of the fetus and the term infant. BMC Pediatr. 2013 Jun 11;13:92. doi: 10.1186/1471-2431-13-92.
Results Reference
background
PubMed Identifier
3174313
Citation
Shennan AT, Dunn MS, Ohlsson A, Lennox K, Hoskins EM. Abnormal pulmonary outcomes in premature infants: prediction from oxygen requirement in the neonatal period. Pediatrics. 1988 Oct;82(4):527-32.
Results Reference
background
PubMed Identifier
20732945
Citation
Stoll BJ, Hansen NI, Bell EF, Shankaran S, Laptook AR, Walsh MC, Hale EC, Newman NS, Schibler K, Carlo WA, Kennedy KA, Poindexter BB, Finer NN, Ehrenkranz RA, Duara S, Sanchez PJ, O'Shea TM, Goldberg RN, Van Meurs KP, Faix RG, Phelps DL, Frantz ID 3rd, Watterberg KL, Saha S, Das A, Higgins RD; Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network. Neonatal outcomes of extremely preterm infants from the NICHD Neonatal Research Network. Pediatrics. 2010 Sep;126(3):443-56. doi: 10.1542/peds.2009-2959. Epub 2010 Aug 23.
Results Reference
background
PubMed Identifier
14754982
Citation
Poets CF. Gastroesophageal reflux: a critical review of its role in preterm infants. Pediatrics. 2004 Feb;113(2):e128-32. doi: 10.1542/peds.113.2.e128.
Results Reference
background
PubMed Identifier
12235066
Citation
Omari TI, Barnett CP, Benninga MA, Lontis R, Goodchild L, Haslam RR, Dent J, Davidson GP. Mechanisms of gastro-oesophageal reflux in preterm and term infants with reflux disease. Gut. 2002 Oct;51(4):475-9. doi: 10.1136/gut.51.4.475.
Results Reference
background
PubMed Identifier
25318633
Citation
Garland JS, Alex CP, Johnston N, Yan JC, Werlin SL. Association between tracheal pepsin, a reliable marker of gastric aspiration, and head of bed elevation among ventilated neonates. J Neonatal Perinatal Med. 2014 Jan 1;7(3):185-92. doi: 10.3233/NPM-14814020.
Results Reference
background
PubMed Identifier
12183728
Citation
Peter CS, Wiechers C, Bohnhorst B, Silny J, Poets CF. Influence of nasogastric tubes on gastroesophageal reflux in preterm infants: a multiple intraluminal impedance study. J Pediatr. 2002 Aug;141(2):277-9. doi: 10.1067/mpd.2002.126298.
Results Reference
background
PubMed Identifier
2380892
Citation
Jolley SG, Halpern CT, Sterling CE, Feldman BH. The relationship of respiratory complications from gastroesophageal reflux to prematurity in infants. J Pediatr Surg. 1990 Jul;25(7):755-7. doi: 10.1016/s0022-3468(05)80012-0.
Results Reference
background
PubMed Identifier
16954956
Citation
Farhath S, Aghai ZH, Nakhla T, Saslow J, He Z, Soundar S, Mehta DI. Pepsin, a reliable marker of gastric aspiration, is frequently detected in tracheal aspirates from premature ventilated neonates: relationship with feeding and methylxanthine therapy. J Pediatr Gastroenterol Nutr. 2006 Sep;43(3):336-41. doi: 10.1097/01.mpg.0000232015.56155.03.
Results Reference
background
PubMed Identifier
15371091
Citation
Knight PR, Davidson BA, Nader ND, Helinski JD, Marschke CJ, Russo TA, Hutson AD, Notter RH, Holm BA. Progressive, severe lung injury secondary to the interaction of insults in gastric aspiration. Exp Lung Res. 2004 Oct-Nov;30(7):535-57. doi: 10.1080/01902140490489162.
Results Reference
background
PubMed Identifier
8496756
Citation
Blondheim O, Abbasi S, Fox WW, Bhutani VK. Effect of enteral gavage feeding rate on pulmonary functions of very low birth weight infants. J Pediatr. 1993 May;122(5 Pt 1):751-5. doi: 10.1016/s0022-3476(06)80021-1.
Results Reference
background
PubMed Identifier
24753497
Citation
Jensen EA, Munson DA, Zhang H, Blinman TA, Kirpalani H. Anti-gastroesophageal reflux surgery in infants with severe bronchopulmonary dysplasia. Pediatr Pulmonol. 2015 Jun;50(6):584-7. doi: 10.1002/ppul.23052. Epub 2014 Apr 21.
Results Reference
background
PubMed Identifier
17636725
Citation
McGuire W, McEwan P. Transpyloric versus gastric tube feeding for preterm infants. Cochrane Database Syst Rev. 2007 Jul 18;(3):CD003487. doi: 10.1002/14651858.CD003487.pub2.
Results Reference
background
PubMed Identifier
807697
Citation
Wells DH, Zachman RD. Nasojejunal feedings in low-birth-weight infants. J Pediatr. 1975 Aug;87(2):276-9. doi: 10.1016/s0022-3476(75)80602-0.
Results Reference
background
PubMed Identifier
114157
Citation
Drew JH, Johnston R, Finocchiaro C, Taylor PS, Goldberg HJ. A comparison of nasojejunal witn nasogastric feedings in low-birth-weight infants. Aust Paediatr J. 1979 Jun;15(2):98-100. doi: 10.1111/j.1440-1754.1979.tb01198.x. No abstract available.
Results Reference
background
PubMed Identifier
402459
Citation
Roy RN, Pollnitz RB, Hamilton JR, Chance GW. Impaired assimilation of nasojejunal feeds in healthy low-birth-weight newborn infants. J Pediatr. 1977 Mar;90(3):431-4. doi: 10.1016/s0022-3476(77)80710-5.
Results Reference
background
PubMed Identifier
6810764
Citation
Whitfield MF. Poor weight gain of the low birthweight infant fed nasojejunally. Arch Dis Child. 1982 Aug;57(8):597-601. doi: 10.1136/adc.57.8.597.
Results Reference
background
PubMed Identifier
20036378
Citation
Sullivan S, Schanler RJ, Kim JH, Patel AL, Trawoger R, Kiechl-Kohlendorfer U, Chan GM, Blanco CL, Abrams S, Cotten CM, Laroia N, Ehrenkranz RA, Dudell G, Cristofalo EA, Meier P, Lee ML, Rechtman DJ, Lucas A. An exclusively human milk-based diet is associated with a lower rate of necrotizing enterocolitis than a diet of human milk and bovine milk-based products. J Pediatr. 2010 Apr;156(4):562-7.e1. doi: 10.1016/j.jpeds.2009.10.040. Epub 2009 Dec 29.
Results Reference
background
PubMed Identifier
3082297
Citation
Laing IA, Lang MA, Callaghan O, Hume R. Nasogastric compared with nasoduodenal feeding in low birthweight infants. Arch Dis Child. 1986 Feb;61(2):138-41. doi: 10.1136/adc.61.2.138.
Results Reference
background
PubMed Identifier
30967655
Citation
Wallenstein MB, Brooks C, Kline TA, Beck RQ, Yang W, Shaw GM, Stevenson DK. Early transpyloric vs gastric feeding in preterm infants: a retrospective cohort study. J Perinatol. 2019 Jun;39(6):837-841. doi: 10.1038/s41372-019-0372-3. Epub 2019 Apr 9.
Results Reference
background
PubMed Identifier
1586185
Citation
Macdonald PD, Skeoch CH, Carse H, Dryburgh F, Alroomi LG, Galea P, Gettinby G. Randomised trial of continuous nasogastric, bolus nasogastric, and transpyloric feeding in infants of birth weight under 1400 g. Arch Dis Child. 1992 Apr;67(4 Spec No):429-31. doi: 10.1136/adc.67.4_spec_no.429.
Results Reference
background
PubMed Identifier
6787557
Citation
Pereira GR, Lemons JA. Controlled study of transpyloric and intermittent gavage feeding in the small preterm infant. Pediatrics. 1981 Jan;67(1):68-72.
Results Reference
background
PubMed Identifier
812052
Citation
Caillie MV, Powell GK. Nasoduodenal versus nasogastric feeding in the very low birthweight infant. Pediatrics. 1975 Dec;56(6):1065-72.
Results Reference
background
PubMed Identifier
19242488
Citation
Malcolm WF, Smith PB, Mears S, Goldberg RN, Cotten CM. Transpyloric tube feeding in very low birthweight infants with suspected gastroesophageal reflux: impact on apnea and bradycardia. J Perinatol. 2009 May;29(5):372-5. doi: 10.1038/jp.2008.234. Epub 2009 Feb 26.
Results Reference
background
PubMed Identifier
17850402
Citation
Misra S, Macwan K, Albert V. Transpyloric feeding in gastroesophageal-reflux-associated apnea in premature infants. Acta Paediatr. 2007 Oct;96(10):1426-9. doi: 10.1111/j.1651-2227.2007.00442.x. Epub 2007 Sep 10.
Results Reference
background
PubMed Identifier
19384225
Citation
Hsu CW, Sun SF, Lin SL, Kang SP, Chu KA, Lin CH, Huang HH. Duodenal versus gastric feeding in medical intensive care unit patients: a prospective, randomized, clinical study. Crit Care Med. 2009 Jun;37(6):1866-72. doi: 10.1097/CCM.0b013e31819ffcda.
Results Reference
background
PubMed Identifier
7813274
Citation
Radford PJ, Stillwell PC, Blue B, Hertel G. Aspiration complicating bronchopulmonary dysplasia. Chest. 1995 Jan;107(1):185-8. doi: 10.1378/chest.107.1.185.
Results Reference
result

Learn more about this trial

Duodenal Feeds in Very Low Birth Weight Infants

We'll reach out to this number within 24 hrs