Respiratory Distress Syndrome, Newborn Clinical Trial
Official title:
Comparison of Efficacy of Noninvasive Ventilation With RAM Cannula Versus Short Bi-nasal Cannula in Respiratory Distress Syndrome of Preterm Infants
| NCT number | NCT03366714 |
| Other study ID # | 2017/40 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | April 1, 2017 |
| Est. completion date | August 15, 2018 |
| Verified date | February 2020 |
| Source | Inonu University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
Noninvasive ventilation defines methods of providing ventilation support with constant or
variable pressure using nasal or nasopharyngeal interfaces without endotracheal intubation or
tracheostomy. Today, short binasal prongs and different types of nasal masks are the most
commonly used nasal interfaces in the NICU with the aim of providing NIV.
RAM cannula (Neotech ™, Valencia, CA), a new nasal interface, is increasingly used in NID
applications in newborn infants. The RAM cannula is available in the inspiration and
expiration arms of the stroke while reducing the dead space in the respiratory tract due to
the low nasal prong diameter. There are not enough studies comparing the effectiveness of the
RAM cannula with other short binasal prongs or nasal masks.
Investigators compared the effectiveness and nasal injury rates of RAM cannula and short
binasal prong as NIV interfaces in preterm infants.
| Status | Completed |
| Enrollment | 100 |
| Est. completion date | August 15, 2018 |
| Est. primary completion date | June 1, 2018 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | N/A to 15 Minutes |
| Eligibility |
Inclusion Criteria: - gestational age between 26-34 weeks and, - born in our hospital and, - Patients with clinical findings (tachypnea, groaning, chest retractions) of RDS Exclusion Criteria: - Patients who needed intubation to stabilize in the delivery room or who had severe congenital anomalies. |
| Country | Name | City | State |
|---|---|---|---|
| Turkey | Turgut Özal Medical Center | Malatya |
| Lead Sponsor | Collaborator |
|---|---|
| Inonu University |
Turkey,
Davis P, Davies M, Faber B. A randomised controlled trial of two methods of delivering nasal continuous positive airway pressure after extubation to infants weighing less than 1000 g: binasal (Hudson) versus single nasal prongs. Arch Dis Child Fetal Neonatal Ed. 2001 Sep;85(2):F82-5. — View Citation
Gerdes JS, Sivieri EM, Abbasi S. Factors influencing delivered mean airway pressure during nasal CPAP with the RAM cannula. Pediatr Pulmonol. 2016 Jan;51(1):60-9. doi: 10.1002/ppul.23197. Epub 2015 Apr 7. — View Citation
Nzegwu NI, Mack T, DellaVentura R, Dunphy L, Koval N, Levit O, Bhandari V. Systematic use of the RAM nasal cannula in the Yale-New Haven Children's Hospital Neonatal Intensive Care Unit: a quality improvement project. J Matern Fetal Neonatal Med. 2015 Apr — View Citation
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Nasal IPPV failure | Non invasive ventilation failure in patients who underwent nasal IPPV with RAM cannula | up to four weeks | |
| Secondary | NIV duration | In patients with NIV (nasal IPPV) who underwent RAM cannula or short binasal cannula (prong). We compared the time of NIV | up to two months |
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