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Rescue High Frequency Oscillatory Ventilation in Newborns Who Do Not Respond to Conventional Ventilation

Rescue High Frequency Oscillatory Ventilation in Newborns Who Do Not Respond to Conventional Ventilation

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02752438
Acronym
RescueHFO
Enrollment
400
Registered
2016-04-27
Start date
2016-05-31
Completion date
2017-07-31
Last updated
2016-09-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Mechanical Ventilatory Failure

Keywords

high frequency oscillatory ventilation, rescue, newborn

Brief summary

Although High Frequency Oscillatory Ventilation (HFOV) has been used in case of unresponsive to conventional mechanical ventilation both in children and newborns, there is no data on its success and the factors that affect its success in the literature.

Detailed description

Although High Frequency Oscillatory Ventilation (HFOV) has been used in case of unresponsive to conventional mechanical ventilation both in children and newborns, there is no data on its success and the factors that affect its success in the literature. The aim of the study is to define the factors that affect the success of HFOV in newborns who do not respond to conventional mechanical ventilation through an online registry among neonatal intensive care units in Turkey.

Interventions

DEVICEHFOV

HFOV is a kind of respiratory support with a rate higher than physiological but with lesser volume.

Sponsors

Saglik Bilimleri Universitesi Gulhane Tip Fakultesi
CollaboratorOTHER
Etlik Zubeyde Hanim Womens
CollaboratorUNKNOWN
Zeynep Kamil Maternity and Pediatric Research and Training Hospital
CollaboratorOTHER
Gazi University
CollaboratorOTHER
Istanbul Medeniyet University
CollaboratorOTHER
Dr. Behcet Uz Children's Hospital
CollaboratorOTHER
Celal Bayar University
CollaboratorOTHER
Special Metro Hospital
CollaboratorOTHER
Konya Meram State Hospital
CollaboratorOTHER
Inonu University
CollaboratorOTHER
Ankara University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Days to 28 Days
Healthy volunteers
No

Inclusion criteria

* patients switched to HFOV in case of unresponse to conventional ventilation * stay on HFOV for at least 4 h

Exclusion criteria

* any congenital anomaly * HFOV duration less then 4 h

Design outcomes

Primary

MeasureTime frame
Survival3 months

Secondary

MeasureTime frame
Cut-off gestational age for survival3 months
Cut-off birthweight for survival3 months

Countries

Turkey (Türkiye)

Contacts

Primary ContactEmel Okulu, Attending
emelokulu@gmail.com5054812151
Backup ContactOmer Erdeve
5054812151

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026