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Comparing the effectiveness of two mask and nasal tube ventilation methods in premature infants with respiratory failure

Comparing the efficacy of NCPAP and NIPPV in premature infants with RDS after extubation in NICU ward of Najmiyeh Hospital

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017050517413N25
Enrollment
60
Registered
2017-06-12
Start date
2015-04-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Respiratory distress syndrome of newborn. Respiratory distress syndrome of newborn

Interventions

Intervention 1: Intervention group: Ventilation by NCPAP. Intervention 2: Control group: Ventilation by NIPPV.
Treatment - Other
Intervention group: Ventilation by NCPAP
Control group: Ventilation by NIPPV

Sponsors

Vice Chancellor for Research, Baqiyatallah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 28 Days

Inclusion criteria

Inclusion criteria: Inclusion criteria:gestational ages of less than 34 weeks ; birthweight of less than 1800 gr; respiratory distress despite receiving Surfactant and mechanical ventilation; needed FIO2 of less than 60% after extubation Exclusion criteria:anomalies in nasopharyngeal path, heart or lungs; chromosomal anomalies; intraventricular hemorrhage (IVH); not willing to participate

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Duration of ventilation. Timepoint: After intervention. Method of measurement: Time record by nurse.;Oxygen Saturation. Timepoint: After intervention. Method of measurement: Pulse Oxymetry.;Arterial oxygen pressure. Timepoint: After intervention. Method of measurement: Arterial Blood Gas Assessment.;Respiratory rate. Timepoint: After intervention. Method of measurement: one minute counting by nurse.

Secondary

MeasureTime frame
Abdominal Distention. Timepoint: After intervention. Method of measurement: Physical examination.;Mortality. Timepoint: After intervention. Method of measurement: Recording mortality cases.;Intraventricular hemorrhage. Timepoint: After intervention. Method of measurement: Brain sonography.;Necrotizing Enterocolitis. Timepoint: After intervention. Method of measurement: Physical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Hossein Khosravi

Student Research Committee, Baqiyatallah University of Medical Sciences, Tehran, Iran

dr.mhkhosravi@gmail.com+98 21 8862 0826

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026