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RAM Cannula VS Short Nasal Prongs for Delivering NIPPV in Preterm Infants (RAMCAN)

R

Rambam Health Care Campus

Status

Completed

Conditions

Intubation, Intratracheal
Noninvasive Ventilation
Respiratory Distress Syndrome, Newborn
Infant, Premature

Treatments

Device: Ram cannula
Device: Short nasal prongs

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Randomized control trial, Ram cannula VS short nasal prongs for delivering Non Invasive Positive Pressure Ventilation (NIPPV) for preterm infants

Full description

Randomized control trial comparing Ram cannula to the regular, more investigated short nasal prongs for delivering Non Invasive Positive Pressure Ventilation (NIPPV) for preterm infants with respiratory distress.

Enrollment

166 patients

Sex

All

Ages

Under 28 days old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Gestational age 24-33.6
  • Physician decision on the need for non invasive ventilation
  • parental consent

Exclusion criteria

  • Pneumothorax before recruitment
  • Significant congenital heart disease or chromosomal disorder

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

166 participants in 2 patient groups

Ram cannula
Experimental group
Description:
NIPPV VIA Ram cannula
Treatment:
Device: Ram cannula
Short nasal prongs
Active Comparator group
Description:
NIPPV VIA short nasal prongs
Treatment:
Device: Short nasal prongs

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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