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Humidified High Flow Nasal Cannula Versus Nasal Intermittent Positive Ventilation in Neonates

Primary Purpose

Respiratory Insufficiency

Status
Unknown status
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
NIPPV
HHFNC
Sponsored by
Gao WeiWei
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Respiratory Insufficiency focused on measuring NIPPV, HHFNC, RDS, neonate

Eligibility Criteria

undefined - 28 Days (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Birth weight > 1000 grams and > 28 weeks gestation
  2. have respiratory distress syndrome and need assistant ventilation

Exclusion Criteria:

  1. Birth weight < 1000 grams
  2. Estimated gestation < 28 weeks
  3. infants have contraindications for use of non-invasive ventilation
  4. Active air leak syndrome
  5. Infants with abnormalities of the upper and lower airways; such as Pierre- Robin, Treacher-Collins, Goldenhar, choanal atresia or stenosis, cleft lip and/or palate, or
  6. Infants with significant abdominal or respiratory malformations including trachea-esophageal fistula, intestinal atresia, omphalocele, gastroschisis, and congenital diaphragmatic hernia.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Active Comparator

    Arm Label

    HHFNC

    NIPPV

    Arm Description

    HHFNC is provided nasal cannula. Ventilator settings:fraction of inspired oxygen (FiO2):21-40%,flow:2-8(litre,L)/min,to maintain arterial blood hemoglobin oxygen saturation ( SaO2) at 90-95% The weaning process is left to the discretion of the attending physician.,when FiO2: 25%,flow:2(litre,L)/min.

    NIPPV is provided via binasal prongs. Ventilator settings:FiO2:21-40%,peak inspiratory pressure( PIP):12-22cm H2O,positive and expiratory pressure(PEEP):5-7cm H2O,Rate:30-60 per minute to maintain SaO2 at 90-95%,The weaning process is left to the discretion of the attending physician,when FiO2: 25%,mean airway pressure (MAP):6cm H2O,R:30 per minute .

    Outcomes

    Primary Outcome Measures

    endotracheal intubation rate
    endotracheal intubation rate assessed within 72 hours after extubation

    Secondary Outcome Measures

    significant apnea
    significant apnea measured by the Colin J definition:6 episodes requiring stimulation in 6 hours or requiring>1 episodes of positive -pressure ventilation
    duration of non-invasive ventilation
    the duration of ventilation measured by total non-invasive ventilation time in HHFNC and NIPPV groups
    air leaks
    air leak assessed by chest X-ray
    full enteral feeding
    full enteral feeding measured by total feeding dose above 120 ml per kilogram one day
    Bronchopulmonary dysplasia
    Bronchopulmonary dysplasia assessed by national institute of child health and human development(NICHD) definition
    necrotizing enterocolitis
    necrotizing enterocolitis assessed by abdominal X-ray and Bell classification
    nasal trauma
    nasal trauma measured by US national pressure Ulcer Advisory Panel(NPUAP)

    Full Information

    First Posted
    May 24, 2015
    Last Updated
    February 22, 2016
    Sponsor
    Gao WeiWei
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02499744
    Brief Title
    Humidified High Flow Nasal Cannula Versus Nasal Intermittent Positive Ventilation in Neonates
    Official Title
    Humidified High Flow Nasal Cannula Versus Nasal Intermittent Positive Ventilation in Neonates as Primary Respiratory Support:a Randomized Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2016
    Overall Recruitment Status
    Unknown status
    Study Start Date
    February 2016 (undefined)
    Primary Completion Date
    May 2017 (Anticipated)
    Study Completion Date
    May 2017 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor-Investigator
    Name of the Sponsor
    Gao WeiWei

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The investigators hypothesize that the Humidified High Flow Nasal Cannula(HHFNC) is effective and safe as primary respiratory support in neonate with respiratory distress syndrome(RDS). It is more convenient in HHFNC combined with kangaroo care.
    Detailed Description
    Today a new nursing principle proposed that is kangaroo care in neonate.Many study showed kangaroo care may reduce pain、decrease the respiratory and heart rate among preterm infant.The recently study show it benefit to Physical Growth and Neurodevelopment. Respiratory failure remains a common problem in the neonatal intensive unit. As reported that early non-invasive ventilation is accompanied by significant improvement in subsequent lung development and alveolation.Nasal continuous positive airway pressure (NCPAP)、nasal intermittent positive pressure ventilation(NIPPV) and humidified high flow via nasal cannulas(HHFNC) are non-invasive ventilation models.But Unfortunately, NIPPV and NCPAP systems are not always easily applied or tolerated in the preterm infants.So it is not convenient in kangaroo care.Recently A meta analysis concluded that NIPPV is more effective than NCPAP in preterms respiratory diseases.Maybe the investigators can reason that NIPPV is effective than HHFNC,but there is limited data about the comparison of NIPPV and HHFNC as primary respiratory support in neonate. The NIPPV group fail definition:1、FiO2>40%、MAP>10 centimeter water column (cm H2O),but SaO2<90%.2、significant abdominal distension.3、PaCO2>60 millimeter of mercury (mmHg)or partial pressure of arterial oxygen (PaO2)<45mmHg.4、severe apnea( definition:>6 episodes requiring stimulation in 6 hours or requiring >1 episodes of positive-pressure ventilation) 5.potential of hydrogen (PH)<7.2 The HHFNC group fail definition:1、FiO2>40%、flow>8 (litre,L)/min,but SaO2<90%.2、significant abdominal distension.3、PaCO2>60mmHg or PaO2<45mmHg.4、severe apnea 5.PH<7.2

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Respiratory Insufficiency
    Keywords
    NIPPV, HHFNC, RDS, neonate

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 1
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    200 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    HHFNC
    Arm Type
    Active Comparator
    Arm Description
    HHFNC is provided nasal cannula. Ventilator settings:fraction of inspired oxygen (FiO2):21-40%,flow:2-8(litre,L)/min,to maintain arterial blood hemoglobin oxygen saturation ( SaO2) at 90-95% The weaning process is left to the discretion of the attending physician.,when FiO2: 25%,flow:2(litre,L)/min.
    Arm Title
    NIPPV
    Arm Type
    Active Comparator
    Arm Description
    NIPPV is provided via binasal prongs. Ventilator settings:FiO2:21-40%,peak inspiratory pressure( PIP):12-22cm H2O,positive and expiratory pressure(PEEP):5-7cm H2O,Rate:30-60 per minute to maintain SaO2 at 90-95%,The weaning process is left to the discretion of the attending physician,when FiO2: 25%,mean airway pressure (MAP):6cm H2O,R:30 per minute .
    Intervention Type
    Device
    Intervention Name(s)
    NIPPV
    Other Intervention Name(s)
    nasal intermittent postive pressure ventilaiton
    Intervention Description
    For infants in the NIPPV-group who "fail"NIPPV (see definition below), need immediate intubation, a invasive "Rescue-Treatment" may be provided. The decision to attempt "Rescue-Treatment", the mode of respiratory support and the ventilator settings used are at the discretion of the attending clinician.
    Intervention Type
    Device
    Intervention Name(s)
    HHFNC
    Other Intervention Name(s)
    Humidified High Flow Nasal Cannula
    Intervention Description
    For infants in the HHFNC-group who "fail"HHFNC (see definition below), need immediate intubation, a invasive "Rescue-Treatment" may be provided. The decision to attempt "Rescue-Treatment", the mode of respiratory support and the ventilator settings used are at the discretion of the attending clinician.
    Primary Outcome Measure Information:
    Title
    endotracheal intubation rate
    Description
    endotracheal intubation rate assessed within 72 hours after extubation
    Time Frame
    3 days
    Secondary Outcome Measure Information:
    Title
    significant apnea
    Description
    significant apnea measured by the Colin J definition:6 episodes requiring stimulation in 6 hours or requiring>1 episodes of positive -pressure ventilation
    Time Frame
    7 days
    Title
    duration of non-invasive ventilation
    Description
    the duration of ventilation measured by total non-invasive ventilation time in HHFNC and NIPPV groups
    Time Frame
    3 months
    Title
    air leaks
    Description
    air leak assessed by chest X-ray
    Time Frame
    3 months
    Title
    full enteral feeding
    Description
    full enteral feeding measured by total feeding dose above 120 ml per kilogram one day
    Time Frame
    3 months
    Title
    Bronchopulmonary dysplasia
    Description
    Bronchopulmonary dysplasia assessed by national institute of child health and human development(NICHD) definition
    Time Frame
    3 months
    Title
    necrotizing enterocolitis
    Description
    necrotizing enterocolitis assessed by abdominal X-ray and Bell classification
    Time Frame
    3 months
    Title
    nasal trauma
    Description
    nasal trauma measured by US national pressure Ulcer Advisory Panel(NPUAP)
    Time Frame
    3 months
    Other Pre-specified Outcome Measures:
    Title
    pain score
    Description
    pain score assessed by neonatal infant pain scale (NIPS)
    Time Frame
    3 months
    Title
    neurodevelopment
    Description
    neurodevelopment assessed by Bayley scale
    Time Frame
    3 months

    10. Eligibility

    Sex
    All
    Maximum Age & Unit of Time
    28 Days
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Birth weight > 1000 grams and > 28 weeks gestation have respiratory distress syndrome and need assistant ventilation Exclusion Criteria: Birth weight < 1000 grams Estimated gestation < 28 weeks infants have contraindications for use of non-invasive ventilation Active air leak syndrome Infants with abnormalities of the upper and lower airways; such as Pierre- Robin, Treacher-Collins, Goldenhar, choanal atresia or stenosis, cleft lip and/or palate, or Infants with significant abdominal or respiratory malformations including trachea-esophageal fistula, intestinal atresia, omphalocele, gastroschisis, and congenital diaphragmatic hernia.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    yang jie, doctor
    Organizational Affiliation
    Guangdong Women and Children Hospital
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
    Citations:
    PubMed Identifier
    23796239
    Citation
    Chidambaram AG, Manjula S, Adhisivam B, Bhat BV. Effect of Kangaroo mother care in reducing pain due to heel prick among preterm neonates: a crossover trial. J Matern Fetal Neonatal Med. 2014 Mar;27(5):488-90. doi: 10.3109/14767058.2013.818974. Epub 2013 Jul 18.
    Results Reference
    background
    PubMed Identifier
    20667921
    Citation
    Gathwala G, Singh B, Singh J. Effect of Kangaroo Mother Care on physical growth, breastfeeding and its acceptability. Trop Doct. 2010 Oct;40(4):199-202. doi: 10.1258/td.2010.090513. Epub 2010 Jul 28.
    Results Reference
    background
    PubMed Identifier
    25613847
    Citation
    Padhi TR, Sareen D, Pradhan L, Jalali S, Sutar S, Das T, Modi RR, Behera UC. Evaluation of retinopathy of prematurity screening in reverse Kangaroo Mother Care: a pilot study. Eye (Lond). 2015 Apr;29(4):505-8. doi: 10.1038/eye.2014.340. Epub 2015 Jan 23.
    Results Reference
    background
    PubMed Identifier
    25347107
    Citation
    Head LM. The effect of kangaroo care on neurodevelopmental outcomes in preterm infants. J Perinat Neonatal Nurs. 2014 Oct-Dec;28(4):290-9; quiz E3-4. doi: 10.1097/JPN.0000000000000062.
    Results Reference
    background
    PubMed Identifier
    14962819
    Citation
    Thomson MA, Yoder BA, Winter VT, Martin H, Catland D, Siler-Khodr TM, Coalson JJ. Treatment of immature baboons for 28 days with early nasal continuous positive airway pressure. Am J Respir Crit Care Med. 2004 May 1;169(9):1054-62. doi: 10.1164/rccm.200309-1276OC. Epub 2004 Feb 12.
    Results Reference
    background
    PubMed Identifier
    17262040
    Citation
    Shoemaker MT, Pierce MR, Yoder BA, DiGeronimo RJ. High flow nasal cannula versus nasal CPAP for neonatal respiratory disease: a retrospective study. J Perinatol. 2007 Feb;27(2):85-91. doi: 10.1038/sj.jp.7211647.
    Results Reference
    background
    PubMed Identifier
    11687052
    Citation
    Davis PG, Lemyre B, de Paoli AG. Nasal intermittent positive pressure ventilation (NIPPV) versus nasal continuous positive airway pressure (NCPAP) for preterm neonates after extubation. Cochrane Database Syst Rev. 2001;(3):CD003212. doi: 10.1002/14651858.CD003212.
    Results Reference
    background
    PubMed Identifier
    16724119
    Citation
    Woodhead DD, Lambert DK, Clark JM, Christensen RD. Comparing two methods of delivering high-flow gas therapy by nasal cannula following endotracheal extubation: a prospective, randomized, masked, crossover trial. J Perinatol. 2006 Aug;26(8):481-5. doi: 10.1038/sj.jp.7211543. Epub 2006 May 25.
    Results Reference
    background

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