Intratracheal Vitamin A Administration With Surfactant for Newborn Respiratory Distress Syndrome (RDS)

This study is not yet open for participant recruitment.
Verified November 2010 by Third Military Medical University
Sponsor:
Information provided by:
Third Military Medical University
ClinicalTrials.gov Identifier:
NCT01265589
First received: December 3, 2010
Last updated: July 25, 2011
Last verified: November 2010

December 3, 2010
July 25, 2011
January 2012
December 2012   (final data collection date for primary outcome measure)
Intratracheal Vitamin A Administration with Surfactant for Newborn Respiratory Distress Syndrome [ Time Frame: 1 year ] [ Designated as safety issue: Yes ]
get the date of infants' reflects with Intratracheal Vitamin A Administration
Same as current
Complete list of historical versions of study NCT01265589 on ClinicalTrials.gov Archive Site
Overall clinical outcomes at Newborn Infants With Respiratory Distress Syndrome [ Time Frame: 13 months ] [ Designated as safety issue: Yes ]
analysis the date and drow a conclusion
Same as current
Not Provided
Not Provided
 
Intratracheal Vitamin A Administration With Surfactant for Newborn Respiratory Distress Syndrome
Intratracheal Vitamin A Administration With Surfactant for Newborn Respiratory Distress Syndrome

To research the effect of vitamin A to newborn respiratory distress syndrome by intratracheal administration with surfactant.

Chronic lung disease (CLD) of prematurity is the major cause of long-term disability of extremely LBW (ELBW) premature infants, and it is the most cost consumptive disease in Neonatal Intensive Care Unit graduates. Vitamin A plays an important role in the development of premature lung. Nevertheless, premature infants are prone to vitamin A deficiency. Oral supplementation of vitamin A does not alter the incidence of CLD in ELBW infants. Intramuscular administration of vitamin A reduced the incidence of CLD. The treatment is considered painful and this way is not routinely practiced. Vitamin A is systemically bioavailable after intratracheal administration with surfactant in an animal model of newborn respiratory distress.

Interventional
Phase 3
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Treatment
  • RDS
  • Infant, Newborn
  • Vitamin A
  • Surfactant
  • Drug: surfactant
    Intratracheal Surfactant Administration without Vitamin A for Newborn Respiratory Distress Syndrome
    Other Name: surfactant
  • Drug: surfactant+vitamin A
    Intratracheal Surfactant Administration with Vitamin A for Newborn Respiratory Distress Syndrome
    Other Name: surfactant+vitamin A
  • Placebo Comparator: I=surfactant
    Intratracheal Surfactant Administration without Vitamin A for Newborn Respiratory Distress Syndrome
    Intervention: Drug: surfactant
  • Experimental: II=surfactant+vitamin A
    Intratracheal Surfactant Administration with Vitamin A for Newborn Respiratory Distress Syndrome
    Intervention: Drug: surfactant+vitamin A
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Not yet recruiting
100
December 2013
December 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • 1.Newborn infants with birth weight >500 gm.
  • 2.Gestational age >24 completed weeks.
  • 3.Intention to manage the infant with non-invasive respiratory support (i.e. no endotracheal tube), where either: 1) the infant is within the first 7 days of life and has never been intubated or has received less than 24 hours of total cumulative intubated respiratory support; 2)the infant is within the first 28 days of life, has been managed with intubated respiratory support for 24 hours or more and is a candidate for extubation followed by non-invasive respiratory support.
  • 4.No known lethal congenital anomaly or genetic syndromes.
  • 5.Signed parental informed consent

Exclusion Criteria:

  • 1.Considered non-viable by clinician (decision not to administer effective therapies)
  • 2.Life-threatening congenital abnormalities including congenital heart disease (excluding patent ductus arteriosis)
  • 3.Infants known to require surgical treatment
  • 4.Abnormalities of the upper and lower airways
  • 5.Neuromuscular disorders
  • 6.Infants who are >28 days old and continue to require mechanical ventilation with an endotracheal tube
Both
up to 28 Days
No
Contact: Heqiang Sun +86 15310303739 sunheqiang1@sina.com
Contact: Yuan Shi, MD +86 23 68757731 petshi530@vip.163.com
China
 
NCT01265589
2011001
Yes
Yuan Shi and Heqiang Sun, Daping Hospital, Third Military Medical University
Third Military Medical University
Not Provided
Study Director: Yuan Shi, MD Department of Pediatrics, Daping Hospital, Third Military Medical University
Third Military Medical University
November 2010

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP