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LISA vs INSURE in the Treatment of Respiratory Distress Syndrome in Preterm Infants

Primary Purpose

Preterm Infants

Status
Not yet recruiting
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Intubate-Surfactant-Extubate(INSURE)
less invasive surfactant administration(LISA)
Sponsored by
Anhui Provincial Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Preterm Infants focused on measuring NRDS, preterm infants, LISA, INSURE

Eligibility Criteria

25 Weeks - 32 Weeks (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Gestational age (GA) less than 32 weeks
  • diagnosis of RDS. The diagnosis of RDS will be based on clinical manifestations (Progressive dyspnea, nasal flaring and or grunting), chest X-ray findings and need for noninvasive ventilation support(fraction of inspired oxygen>40%) in 6 hours after birth
  • informed parental consent has been obtained

Exclusion Criteria:

  • severe RDS have been treated with endotracheal intubation,surfactant and mechanical ventilation
  • major congenital malformations or complex congenital heart disease
  • Pulmonary hemorrhage
  • Cardiopulmonary failure
  • septicemia, Intraventricular Hemorrhage (IVH, ≥ Grade Ⅲ), and Congenital genetic metabolic disease
  • transferred out of the NICUs(neonatal intensive care units) with surgical treatment or other intervention

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Experimental

    Arm Label

    INSURE

    LISA

    Arm Description

    Intubate-Surfactant-Extubate(INSURE) technique is a Important treatment in premature infants with RDS.

    Less invasive surfactant administration(LISA) technique is a Important treatment in premature infants with RDS.

    Outcomes

    Primary Outcome Measures

    Rate of intubation
    The criteria for endotracheal mechanical ventilation were as follows: severe apnea and bradycardia (defined as recurrent apnea with > 3 episodes per hour associated with heart rate < 100/min, a single episode of apnea that required bag and mask ventilation), hypoxia (FiO2>0.6 with PaO2<50mmHg or TcSO<0.85), severe respiratory acidosis (PaCO2 > 60 mmHg with pH<7.20).
    The incidence of bronchopulmonary dysplasia
    BPD was diagnosed and classified based on the Practical neonatology 4th edition:Need for O2 supplementation(FiO2>0.21) for at least 28 days after birth.

    Secondary Outcome Measures

    Effect on of arterial blood gas analysis
    The improvement of PaO2 and PaCO2 in two groups children with LISA technique
    The Incidence of Patent ductus arteriosus
    PDA was diagnosed based on echocardiography
    The Incidence of Pneumothorax
    Pneumothorax was diagnosed based on clinical manifestations and features of chest x-ray
    The Incidence of Abdominal Distention
    Abdominal circumference was measured 3 times a day during non-invasive ventilation
    The Incidence of Neonatal Necrotizing Enterocolitis(>Stage II)
    Neonatal Necrotizing Enterocolitis was diagnosed by clinical manifestations and features of abdominal x-Ray based on the Practical neonatology 4th edition
    The Incidence of Retinopathy of Prematurity( ≥ Stage II)
    The criteria for Retinopathy of prematurity (>Stage II); extraretinal fibrovascular proliferation neovascularization extends from ridge into the vitreous.
    The Incidence of Intraventricular Hemorrhage (IVH, ≥ Grade Ⅲ)
    The criteria for intraventricular hemorrhage (IVH, ≥ grade Ⅲ): intraventricular hemorrhage with ventricular dilatation and intraventricular hemorrhage with paren-ehymal hemorrhage.
    The Incidence of Periventricular Leukomalacia
    Periventricular Leukomalacia was diagnosed based on cranial MRI
    Predischarge Mortality
    The Time of Non-invasive Ventilation
    Hours
    Days on supplemental oxygen
    Days
    Length of Hospitalization
    Days

    Full Information

    First Posted
    October 4, 2019
    Last Updated
    October 13, 2019
    Sponsor
    Anhui Provincial Hospital
    Collaborators
    The First Affiliated Hospital of University of Science and Technology of China, First Affiliated Hospital Bengbu Medical College, Second Affiliated Hospital of Bengbu Medical College, Fuyang people's hospital, lixin people's hospital, The third people's hospital of bengbu, Huaibei coal general hospital, Bozhou people's hospital, Luan people's hospital, Huaibei maternal and child health hospital, Huainan maternal and child health hospital, Chizhou people's hospital, Xuancheng people's hospital, The affiliated hospital of wannan medical college, Tongling People's Hospital, Maanshan maternity and child care, Wuhu first people's hospital, Anqing Municipal Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04126382
    Brief Title
    LISA vs INSURE in the Treatment of Respiratory Distress Syndrome in Preterm Infants
    Official Title
    The Efficacy of LISA Technology With Noninvasive Ventilation in the Treatment of Respiratory Distress Syndrome in Preterm Neonates
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2019
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    January 1, 2020 (Anticipated)
    Primary Completion Date
    December 31, 2024 (Anticipated)
    Study Completion Date
    December 31, 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Anhui Provincial Hospital
    Collaborators
    The First Affiliated Hospital of University of Science and Technology of China, First Affiliated Hospital Bengbu Medical College, Second Affiliated Hospital of Bengbu Medical College, Fuyang people's hospital, lixin people's hospital, The third people's hospital of bengbu, Huaibei coal general hospital, Bozhou people's hospital, Luan people's hospital, Huaibei maternal and child health hospital, Huainan maternal and child health hospital, Chizhou people's hospital, Xuancheng people's hospital, The affiliated hospital of wannan medical college, Tongling People's Hospital, Maanshan maternity and child care, Wuhu first people's hospital, Anqing Municipal Hospital

    4. Oversight

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

    5. Study Description

    Brief Summary
    To evaluate the efficacy of less invasive surfactant administration(LISA )technique in the treatment of neonatal respiratory distress syndrome(NRDS) by comparing with the traditional Intubate-Surfactant-Extubate(INSURE) technique.
    Detailed Description
    Background: Neonatal Respiratory distress syndrome (NRDS) is the most common cause of respiratory problems in premature babies. Surfactant administration involved with endotracheal intubation and mechanical ventilation has proven to be a effective treatment, however, it is associated with a risk of barotrauma, volutrauma and bronchopulmonary dysplasia(BPD). In recent years, some studies have demonstrated that prophylactic INSURE did not lead to a higher survival without BPD, and LISA technique is recommended. However there is no multicenter and Large sample research about it. The aim of this multicenter trial is to compare the efficacy between LISA-treated and INSURE-treated premature Preterm babies with respiratory distress syndrome(RDS). Methods/Design:In this multicenter, randomized, cohort, prospective trial, 200 preterm infants from 18 neonatal intensive care units in AnHui province whose gestational age (GA) less than 32 weeks with a diagnosis of RDS will be randomized to LISA-treated group and INSURE-treated group. The primary outcomes include rate of intubation,incidence of bronchopulmonary dysplasia(BPD).The secondary outcomes include arterial blood gas analysis,severity of RDS,the incidence of Patent ductus arteriosus(PDA),Pneumothorax,Abdominal Distention,Neonatal Necrotizing Enterocolitis(NEC,>Stage II), Retinopathy of Prematurity( ROP,≥ Stage II), Intraventricular Hemorrhage (IVH, ≥ Grade Ⅲ), Periventricular Leukomalacia(PVL) , mortality, days on noninvasive respiratory support,days on supplemental oxygen and days of hospitalization.Other secondary outcomes include scores of Gesell development Scales of infant development at 3 years of corrected age.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Preterm Infants
    Keywords
    NRDS, preterm infants, LISA, INSURE

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    200 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    INSURE
    Arm Type
    Active Comparator
    Arm Description
    Intubate-Surfactant-Extubate(INSURE) technique is a Important treatment in premature infants with RDS.
    Arm Title
    LISA
    Arm Type
    Experimental
    Arm Description
    Less invasive surfactant administration(LISA) technique is a Important treatment in premature infants with RDS.
    Intervention Type
    Procedure
    Intervention Name(s)
    Intubate-Surfactant-Extubate(INSURE)
    Intervention Description
    Infants are given an endotracheal intubation, with manual lung inflation in order to keep the oxygen supply,and the surfactant(kelisu,China Resources Shuanghe Pharmaceutical) was slowly instilled into the airway through the tracheal tube, and the tracheal tube was removed for non-invasive NCPAP(nasal continuous positive airway pressure)-assisted breathing.
    Intervention Type
    Procedure
    Intervention Name(s)
    less invasive surfactant administration(LISA)
    Intervention Description
    Infants are spontaneously breathing with nasal CPAP(continuous positive airway pressure) support without manual lung inflation and surfactant(kelisu,China Resources Shuanghe Pharmaceutical) is administered through vocal cords via a smaller catheter.
    Primary Outcome Measure Information:
    Title
    Rate of intubation
    Description
    The criteria for endotracheal mechanical ventilation were as follows: severe apnea and bradycardia (defined as recurrent apnea with > 3 episodes per hour associated with heart rate < 100/min, a single episode of apnea that required bag and mask ventilation), hypoxia (FiO2>0.6 with PaO2<50mmHg or TcSO<0.85), severe respiratory acidosis (PaCO2 > 60 mmHg with pH<7.20).
    Time Frame
    during the first 3 days after birth
    Title
    The incidence of bronchopulmonary dysplasia
    Description
    BPD was diagnosed and classified based on the Practical neonatology 4th edition:Need for O2 supplementation(FiO2>0.21) for at least 28 days after birth.
    Time Frame
    at a post-menstrual age of 36 weeks or at discharge
    Secondary Outcome Measure Information:
    Title
    Effect on of arterial blood gas analysis
    Description
    The improvement of PaO2 and PaCO2 in two groups children with LISA technique
    Time Frame
    during the whole procedure of surfactant replacement,up to 3 days after birth
    Title
    The Incidence of Patent ductus arteriosus
    Description
    PDA was diagnosed based on echocardiography
    Time Frame
    during hospitalization, up to 60 days
    Title
    The Incidence of Pneumothorax
    Description
    Pneumothorax was diagnosed based on clinical manifestations and features of chest x-ray
    Time Frame
    during non-invasive ventilation, up to 30 days
    Title
    The Incidence of Abdominal Distention
    Description
    Abdominal circumference was measured 3 times a day during non-invasive ventilation
    Time Frame
    during non-invasive ventilation, up to 30 days
    Title
    The Incidence of Neonatal Necrotizing Enterocolitis(>Stage II)
    Description
    Neonatal Necrotizing Enterocolitis was diagnosed by clinical manifestations and features of abdominal x-Ray based on the Practical neonatology 4th edition
    Time Frame
    during hospitalization, up to 60 days
    Title
    The Incidence of Retinopathy of Prematurity( ≥ Stage II)
    Description
    The criteria for Retinopathy of prematurity (>Stage II); extraretinal fibrovascular proliferation neovascularization extends from ridge into the vitreous.
    Time Frame
    at a post-menstrual age of 36 weeks or at discharge
    Title
    The Incidence of Intraventricular Hemorrhage (IVH, ≥ Grade Ⅲ)
    Description
    The criteria for intraventricular hemorrhage (IVH, ≥ grade Ⅲ): intraventricular hemorrhage with ventricular dilatation and intraventricular hemorrhage with paren-ehymal hemorrhage.
    Time Frame
    during hospitalization, up to 60 days
    Title
    The Incidence of Periventricular Leukomalacia
    Description
    Periventricular Leukomalacia was diagnosed based on cranial MRI
    Time Frame
    during hospitalization, up to 36 months
    Title
    Predischarge Mortality
    Time Frame
    during hospitalization, up to 60 days
    Title
    The Time of Non-invasive Ventilation
    Description
    Hours
    Time Frame
    during hospitalization, up to 60 days
    Title
    Days on supplemental oxygen
    Description
    Days
    Time Frame
    during hospitalization, up to 60 days
    Title
    Length of Hospitalization
    Description
    Days
    Time Frame
    during hospitalization, up to 60 days

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    25 Weeks
    Maximum Age & Unit of Time
    32 Weeks
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Gestational age (GA) less than 32 weeks diagnosis of RDS. The diagnosis of RDS will be based on clinical manifestations (Progressive dyspnea, nasal flaring and or grunting), chest X-ray findings and need for noninvasive ventilation support(fraction of inspired oxygen>40%) in 6 hours after birth informed parental consent has been obtained Exclusion Criteria: severe RDS have been treated with endotracheal intubation,surfactant and mechanical ventilation major congenital malformations or complex congenital heart disease Pulmonary hemorrhage Cardiopulmonary failure septicemia, Intraventricular Hemorrhage (IVH, ≥ Grade Ⅲ), and Congenital genetic metabolic disease transferred out of the NICUs(neonatal intensive care units) with surgical treatment or other intervention
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Zhang Lan, PhD
    Phone
    18256935186
    Email
    moaana@163.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Pan Jiahua, PhD
    Phone
    13866167758
    Email
    panjiahua1960@163.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Pan jiahua, PhD
    Organizational Affiliation
    Director of pediatric department of the First Affiliated Hospital of University of Science and Technology of China
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

    Learn more about this trial

    LISA vs INSURE in the Treatment of Respiratory Distress Syndrome in Preterm Infants

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