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Comparison between two ventilatory modes in reducing the days of mechanical ventilation and also assosciated complications.

Not Applicable
Completed
Conditions
Health Condition 1: null- Prematurely born newborns with Respiratory distress syndrome
Registration Number
CTRI/2017/11/010439
Lead Sponsor
I
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
81
Inclusion Criteria

1 Neonates with congenital cyanotic heart diseases.

2 Neonates with major congenital malformations.

3 Neonates with air leak syndromes.

4 Neonates requiring High Frequency Oscillatory Ventilation (HFOV)

Exclusion Criteria

1.Neonates with congenital cyanotic heart diseases.

2.Neonates with major congenital malformations.

3.Neonates with air leak syndromes.

4.Neonates requiring High Frequency Oscillatory Ventilation (HFOV)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Primary outcome is to compare the time required to reach the weaning criteria assessed by volume targeted ventilation to pressure limited ventilation in prematurely born infants.Timepoint: At the time of extubation
Secondary Outcome Measures
NameTimeMethod
1 Rate of failure <br/ ><br>2 Oxygenation Index at 6th hourly <br/ ><br>3 FiO2 to SpO2 ratio <br/ ><br>4 PaO2 to FiO2 ratio <br/ ><br>5 Episodes of hypocarbia at 2nd hourly <br/ ><br>6 Duration of mechanical ventilation <br/ ><br>7 Oxygen radicals <br/ ><br>8 Complications such as <br/ ><br>9 Broncho pulmonary dysplasia(BPD) <br/ ><br>10 Periventricular leukomalacia(PVL) <br/ ><br>11 Air leak syndrome <br/ ><br>12 Intraventricular Hemorrhage (IVH) <br/ ><br>13 Retinopathy of Prematurity (ROP) <br/ ><br>14 Mortality <br/ ><br>Timepoint: at the time of extubation and at the time of discharge
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