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
About this trial
This is an interventional treatment trial for Preterm Infants focused on measuring NRDS, preterm infants, LISA, INSURE
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
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
NCT ID
NCT04126382
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
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
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LISA vs INSURE in the Treatment of Respiratory Distress Syndrome in Preterm Infants
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