Observational Study in Preterm Neonates Who Are Sufficiently Stable on Non-Invasive Ventilatory Support

Completed

• Conditions: Infant Respiratory Distress Syndrome; Non-invasive Ventilatory Support
• Interventions: Other: Preterm Neonates

• Registration Number: NCT01861795
• Lead Sponsor: Takeda

Brief Summary

The purpose of this observational study is to collect data on vital signs, oxygen requirements and other data related to ventilator care in preterm neonates under standard of care treatment.

Detailed Description

The objective of this study is to collect data on vital signs, oxygen requirements and other data in preterm infants who are breathing stably on non-invasive ventilatory support. The data obtained during this study will be used to compare data obtained in a future study that will add a new medicinal product in combination with non-invasive ventilatory support to accelerate lung development in preterm infants.

The study will enroll approximately 40 patients. Participants will not be receiving any investigational medicinal product or device in this study.

All participants will have vital signs, oxygen requirements and other data collected continuously throughout the study.

This multi-centre trial will be conducted in Germany. The overall time to participate in this study is up to 10 weeks. Participants will be observed until they reach 36 weeks of gestational age or until they are discharged from the hospital.

Study Timeline

• Study First Submitted: 2013-04-26
• Study First Submitted QC: 2013-05-21
• Study First Posted: 2013-05-24
• Study Start: 2013-06
• Primary Completion: 2014-03
• Study Completion: 2014-03
• Status Verified: 2014-08
• Last Update Submitted: 2014-08-20
• Last Update Posted: 2014-08-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• 1. Written, informed consent of both parents or legal guardian(s) obtained (on admission, prior to or after delivery).

  2. Preterm neonates born at or above 27+0 gestational weeks (GW) who are sufficiently stable on nasal continuous positive airway pressure (CPAP). Upper limit 36+0 GW.

  3. Participants' minimum weight at birth must be 800 g. Upper weight limit is 2500 g.

  4. CPAP-positive end-expiratory pressure (PEEP) must be ≥5 cm and ≤ 8 cm H2O. 5. Fraction of oxygen (O2) in ventilator outlet gas flow (FiO2) ≥ 30% to reach saturation goal (SpO2 between 88% and 96%) during the time period from B0 to T0.

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Exclusion Criteria

• 1. FiO2 > 50% to reach saturation goal (saturation of peripheral oxygen (SpO2) between 88% and 96%) during the time period from 30 minutes after birth (B0) to 45 minutes after birth (T0).

  2. Presence of severe respiratory distress syndrome (RDS) necessitating immediate intubation and surfactant rescue at entry into the study, or having necessitated surfactant rescue prior to entry into the study.

  3. Known life-threatening congenital anomaly or genetic syndrome. 4. Participation in an interventional study in parallel to this observational study.

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Preterm Neonates	Preterm Neonates	Preterm neonates born at or above 27+0 weeks of gestational age sufficiently stable on nasal continuous positive airway pressure (CPAP) will be treated by standard of care.

Primary Outcome Measures

Name	Time	Method
Time and failure-adjusted Area Under the Curve (AUC) from Time 0 (T0) to 98 hours after T0 (T47) (AUCT0-T47adjusted) of fraction of inspired oxygen (FiO2)	Beginning of the Intensive observation phase (T0; approximately 45 minutes after birth) to 98 hours after T0	Fraction of inspired oxygen (FiO2) is the amount of oxygen in the ventilator outlet gas flow.

Secondary Outcome Measures

Name	Time	Method
Continuous positive airway pressure (CPAP)-failure necessitating intubation and mechanical ventillation and/or surfactant instillation during observation period from T0 to 98 hours	T0 to 98 hours	CPAP failure is reached when FiO2 ≥ 50% is need for more than 15 minutes to reach 90% saturation of peripheral oxygen (SpO2).
Percentage of participants requiring instillation of an approved surfactant preparation	Gestational week (GW) 36+6 days
Mortality rate	T0 to Gestational Week 36+6 days
Time of additional oxygen demand (FiO2 > 21%)	T0 to Gestational Week 36+6 days
Time with optimal saturation of peripheral oxygen (SpO2) of 88% to 96%	T0 and at 0.25, 0.5, 0.75 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75 4, 4.25. 4.5, 4.74, 5, 5.25, 5.75, 6, 10, 14, 18, 22, 26, 30, 34, 38, 42, 46, 50, and 54 hours	Saturation of peripheral oxygen is the amount of oxygen bound to hemoglobin in the blood expressed as a percentage of the maximal binding capacity. It will be measured with a pulse oximeter.
Time under Continuous Positive Airway Pressure ventilatory support	T0 to Gestational Week 36+6 days
Time on any ventilation support	T0 to Gestational Week 36+6 days	Any ventilation support includes continuous positive airway pressure (CPAP), manual support and intubation.
Percentage of participants with bronchopulmonary dysplasia (BPD) at GW 36	Gestational Week 36	Bronchopulmonary dysplasia (BPD) is defined as a lung injury in preterm neonates resulting from oxygen toxicity and/or mechanical ventilation (elevated air pressure).
Respiratory rate over time	T0 to Gestational Week 36
Percentage of participants with a positive room-air challenge test at Gestational Week 36	Gestational Week 36	The room-air challenge test is defined as a weaning attempt allowing the participant to breath non-pressurized room air for 30 minutes. If a blood oxygen saturation of ≥90% is achieved during weaning, the weaning was successful and patients are considered to be free of bronchopulmonary dysplasia and need no further ventilation support.
Time in neonatal intensive care unit (NICU) or intermediate care unit (IMCU)	T0 to Gestational Week 36+6 days
Time of intubation for mechanical ventilation	T0 to Gestational Week 36+6 days
Days in hospital	From T0 to Gestational Week 36+6 days