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Surfactant Application During Spontaneous Breathing With Continuous Positive Airway Pressure (CPAP) in Premature Infants < 27 Weeks (NINSAPP)

Primary Purpose

Respiratory Distress Syndrome, Newborn

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Curosurf
Curosurf
Sponsored by
University of Cologne
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Respiratory Distress Syndrome, Newborn focused on measuring Continuous positive airway pressure (CPAP), extremely preterm infant, Idiopathic respiratory distress syndrome (IRDS), Surfactant

Eligibility Criteria

23 Weeks - 26 Weeks (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • IRDS with Silverman-Score ≥ 5 and / or FiO2 ≥ 0,3
  • Postnatal age of more than 10 min. and less than 2 hours
  • Gestational age ≥ 23+0 and < 27+0

Exclusion Criteria:

  • Primary cardio- pulmonary resuscitation
  • Prenatally diagnosed severe malformation
  • No parental consent
  • Participation in another interventional trial

Sites / Locations

  • Klinikum Aschaffenburg, Klinik für Kinder- und Jugendmedizin
  • Charité
  • Ruhr University of Bochum, Children's Hospital St. Josef Spital
  • University Hospital, Dept. of Neonatology
  • Kliniken der Stadt Koeln, Kinderkrankenhaus Riehl
  • University of Cologne, Clinic for Paediatrics
  • Vestische Kinder- und Jugendklinik
  • University Hospital, Clinic for Paediatrics
  • Asklepios Klinik Barmbek
  • Hospital of Leverkusen, Dept. of Children's Medicine
  • University Hospital of Schleswig-Holstein, Campus Lübeck, Dept. of Children's Medicine
  • DRK Kinderklinik
  • Klinikum Stuttgart, Olgahospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

2

1

Arm Description

Conventional therapy with intubation, initiation of mechanical ventilation and surfactant application

Surfactant application via a thin endotracheal catheter during spontaneous breathing with CPAP, followed by respiratory support with CPAP

Outcomes

Primary Outcome Measures

Survival until term without CLD

Secondary Outcome Measures

Survival until term without CLD, IVH>II°, cystic PVL, ROP with need for surgery

Full Information

First Posted
September 11, 2008
Last Updated
July 18, 2012
Sponsor
University of Cologne
Collaborators
University Hospital Schleswig-Holstein, Altona Children's Hospital, Ruhr University of Bochum, Vestische Kinder- und Jugendklinik Datteln, Hospital of Leverkusen, Kliniken der Stadt Koeln, Kinderkrankenhaus Riehl, Heinrich-Heine University, Duesseldorf, Klinikum Aschaffenburg-Alzenau, Asklepios Kliniken Hamburg GmbH, Klinikum Stuttgart, DRK Kinderklinik Siegen, University Hospital, Bonn, Charite University, Berlin, Germany, The Clinical Trials Centre Cologne, German Federal Ministry of Education and Research
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1. Study Identification

Unique Protocol Identification Number
NCT00751959
Brief Title
Surfactant Application During Spontaneous Breathing With Continuous Positive Airway Pressure (CPAP) in Premature Infants < 27 Weeks
Acronym
NINSAPP
Official Title
Surfactant Application During Spontaneous Breathing With CPAP or During Mechanical Ventilation in the Therapy of IRDS in Premature Infants < 27 Weeks
Study Type
Interventional

2. Study Status

Record Verification Date
July 2012
Overall Recruitment Status
Completed
Study Start Date
April 2009 (undefined)
Primary Completion Date
June 2012 (Actual)
Study Completion Date
June 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Cologne
Collaborators
University Hospital Schleswig-Holstein, Altona Children's Hospital, Ruhr University of Bochum, Vestische Kinder- und Jugendklinik Datteln, Hospital of Leverkusen, Kliniken der Stadt Koeln, Kinderkrankenhaus Riehl, Heinrich-Heine University, Duesseldorf, Klinikum Aschaffenburg-Alzenau, Asklepios Kliniken Hamburg GmbH, Klinikum Stuttgart, DRK Kinderklinik Siegen, University Hospital, Bonn, Charite University, Berlin, Germany, The Clinical Trials Centre Cologne, German Federal Ministry of Education and Research

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study investigates the efficacy of surfactant application during spontaneous breathing with CPAP in avoiding death and chronic lung disease (CLD) in very immature infants with a gestational age of less than 27 weeks.
Detailed Description
80 % of extremely preterm infants with a gestational age of less than 27 completed weeks suffer from severe idiopathic respiratory distress syndrome (IRDS). They are still at high risk of mortality and long term morbidity especially of the lung and the brain. At least death and chronic lung disease (CLD) are related to the need and the duration of mechanical ventilation. Continuous positive airway pressure (CPAP) has been shown to be effective to avoid mechanical ventilation in the treatment of IRDS but it often fails in the most immature infants. Early or prophylactic surfactant application is effective in the treatment of IRDS and is the only causal therapy, but it is usually related to intubation and mechanical ventilation that should be avoided.Therefore to overcome the dilemma between need for mechanical ventilation with surfactant administration on the one hand and surfactant withholding with the use of CPAP on the other hand, a strategy was developed to administer surfactant during spontaneous breathing with CPAP (1). In the proposed prospective randomised controlled trial this strategy shall be compared with the recent gold standard in the therapy of extremely preterm infants with IRDS, that is intubation, mechanical ventilation and surfactant administration. Based on the results of a feasibility (1) study and some clinical observations it is hypothesised that the new approach is superior in avoidance of death and chronic lung disease compared to the recent gold standard.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Respiratory Distress Syndrome, Newborn
Keywords
Continuous positive airway pressure (CPAP), extremely preterm infant, Idiopathic respiratory distress syndrome (IRDS), Surfactant

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
213 (Actual)

8. Arms, Groups, and Interventions

Arm Title
2
Arm Type
Active Comparator
Arm Description
Conventional therapy with intubation, initiation of mechanical ventilation and surfactant application
Arm Title
1
Arm Type
Experimental
Arm Description
Surfactant application via a thin endotracheal catheter during spontaneous breathing with CPAP, followed by respiratory support with CPAP
Intervention Type
Drug
Intervention Name(s)
Curosurf
Intervention Description
Surfactant application via a thin endotracheal catheter during spontaneous breathing with CPAP, followed by respiratory support with CPAP
Intervention Type
Drug
Intervention Name(s)
Curosurf
Intervention Description
Conventional therapy with intubation, initiation of mechanical ventilation and surfactant application
Primary Outcome Measure Information:
Title
Survival until term without CLD
Time Frame
13-17 weeks after birth
Secondary Outcome Measure Information:
Title
Survival until term without CLD, IVH>II°, cystic PVL, ROP with need for surgery
Time Frame
13-17 weeks after birth

10. Eligibility

Sex
All
Minimum Age & Unit of Time
23 Weeks
Maximum Age & Unit of Time
26 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: IRDS with Silverman-Score ≥ 5 and / or FiO2 ≥ 0,3 Postnatal age of more than 10 min. and less than 2 hours Gestational age ≥ 23+0 and < 27+0 Exclusion Criteria: Primary cardio- pulmonary resuscitation Prenatally diagnosed severe malformation No parental consent Participation in another interventional trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Angela Kribs, MD
Organizational Affiliation
University of Cologne, Clinic for Paediatrics
Official's Role
Principal Investigator
Facility Information:
Facility Name
Klinikum Aschaffenburg, Klinik für Kinder- und Jugendmedizin
City
Aschaffenburg
ZIP/Postal Code
D-63739
Country
Germany
Facility Name
Charité
City
Berlin
ZIP/Postal Code
D-13353
Country
Germany
Facility Name
Ruhr University of Bochum, Children's Hospital St. Josef Spital
City
Bochum
ZIP/Postal Code
D-44791
Country
Germany
Facility Name
University Hospital, Dept. of Neonatology
City
Bonn
ZIP/Postal Code
D-53113
Country
Germany
Facility Name
Kliniken der Stadt Koeln, Kinderkrankenhaus Riehl
City
Cologne
ZIP/Postal Code
50735
Country
Germany
Facility Name
University of Cologne, Clinic for Paediatrics
City
Cologne
ZIP/Postal Code
D-50937
Country
Germany
Facility Name
Vestische Kinder- und Jugendklinik
City
Datteln
ZIP/Postal Code
D-45711
Country
Germany
Facility Name
University Hospital, Clinic for Paediatrics
City
Duesseldorf
ZIP/Postal Code
D-40225
Country
Germany
Facility Name
Asklepios Klinik Barmbek
City
Hamburg
ZIP/Postal Code
D-22291
Country
Germany
Facility Name
Hospital of Leverkusen, Dept. of Children's Medicine
City
Leverkusen
ZIP/Postal Code
D-51375
Country
Germany
Facility Name
University Hospital of Schleswig-Holstein, Campus Lübeck, Dept. of Children's Medicine
City
Lübeck
ZIP/Postal Code
D-23538
Country
Germany
Facility Name
DRK Kinderklinik
City
Siegen
ZIP/Postal Code
D-57072
Country
Germany
Facility Name
Klinikum Stuttgart, Olgahospital
City
Stuttgart
ZIP/Postal Code
D-70196
Country
Germany

12. IPD Sharing Statement

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Surfactant Application During Spontaneous Breathing With Continuous Positive Airway Pressure (CPAP) in Premature Infants < 27 Weeks

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