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Completed

NCT Number: NCT00751959

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

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.

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Key information

Age range

23 week–26 week

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Klinikum Aschaffenburg, Klinik für Kinder- und Jugendmedizin, Aschaffenburg, Germany

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Curosurf

Drug

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

Primary outcomes

  1. Survival until term without CLD

    Time frame: 13-17 weeks after birth

Secondary outcomes

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

    Time frame: 13-17 weeks after birth

Sponsors and collaborators

Lead sponsor

University of Cologne

Other

Collaborators

  • Altona Children's Hospital
  • Asklepios Kliniken Hamburg GmbH
  • Charite University, Berlin, Germany
  • DRK Kinderklinik Siegen
  • German Federal Ministry of Education and Research
  • Heinrich-Heine University, Duesseldorf
  • Hospital of Leverkusen
  • Kliniken der Stadt Koeln, Kinderkrankenhaus Riehl
  • Klinikum Aschaffenburg-Alzenau
  • Klinikum Stuttgart
  • Ruhr University of Bochum
  • The Clinical Trials Centre Cologne
  • University Hospital Schleswig-Holstein - Lübeck Campus
  • University Hospital, Bonn
  • Vestische Kinder- und Jugendklinik Datteln

Registry information

Official study title

Surfactant Application During Spontaneous Breathing With CPAP or During Mechanical Ventilation in the Therapy of IRDS in Premature Infants < 27 Weeks

Acronym: NINSAPP

Important dates

Study start
2009
Primary completion
2012
Study completion
2012
First posted
Sep 12, 2008
Registry last updated
Jul 19, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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