A Multicentered Study on Efficiency of Noninvasive Ventilation Procedures

NCT03066934 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 352

Last updated 2019-09-10

No results posted yet for this study

Summary

Noninvasive ventilation (NIV) is an alternative form of ventilatory support in critical care encompassing different modes of ventilation such as continuous positive airway pressure (CPAP), bilevel positive airway pressure (BiPAP) and high flow nasal cannula ventilation. Although numerous studies on adults exit in literature, the aspects of this ventilatory support is limited in pediatric age groups. Early recognition of respiratory failure and initiation of NIV in a pediatric patient would positively affect prognosis by avoiding certain complications of endotracheal intubation and mechanical ventilation and adds certain advantages. Decreasing re-intubation rates for the ones who are extubated but necessitating further oxygen support is another advantage of NIV. Although numerous studies on adults exit in literature, the aspects of this ventilatory support is limited in pediatric age groups. Besides, success as well as failure and complication rates in pediatric age groups vary extensively. This multi-centered, prospective cohort study is planned to observe the epidemiologic perspectives of study group within underlying problems, success rates between different age groups, complication and re-intubation rates and finally its' effect on prognosis and long term survival in a year period. Hence we believe results of this study would allow us to improve our knowledge on using this technique, applying different modes and parameters appropriately and design criteria to guide clinician in deciding which group of patients would benefit from NIV techniques.

Conditions

  • Noninvasive Positive Pressure Ventilation
  • High Flow Nasal Cannula
  • Failure, Respiratory

Interventions

OTHER

noninvasive ventilation respiratory support

Sponsors & Collaborators

  • Ankara University

    collaborator OTHER
  • Cukurova University

    collaborator OTHER
  • Dokuz Eylul University

    collaborator OTHER
  • Ege University

    collaborator OTHER
  • Izmir Katip Celebi University

    collaborator OTHER
  • TC Erciyes University

    collaborator OTHER
  • Marmara University

    collaborator OTHER
  • Koç University

    collaborator OTHER
  • Ondokuz Mayıs University

    collaborator OTHER
  • Akdeniz University

    lead OTHER

Principal Investigators

  • Oguz Dursun, Asc. Prof. · Akdeniz University Faculty of Mediciane

Eligibility

Min Age
1 Month
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-11-30
Primary Completion
2017-12-31
Completion
2018-11-30

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03066934 on ClinicalTrials.gov