Automated versus Manual modification of Oxygen in premature newborn on respiratory support: a clinical trial
- Conditions
- Health Condition 1: J962- Acute and chronic respiratory failure
- Registration Number
- CTRI/2022/07/044483
- Lead Sponsor
- Prithiviraj Kesavan
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
1. Neonates who are <44 weeks post-menstrual age irrespective of day of life and day of hospital stay 2. Receiving respiratory support through mechanical ventilator irrespective of the mode of ventilation (both non-invasive and invasive modes of ventilation)with auto Fio2 3. Requiring supplemental oxygen greater than 25%
1. Major or life-threatening congenital anomalies
2. Hemodynamic instability requiring vasopressors or inotropes or inhaled nitric oxide
3. Culture proven sepsis or Meningitis within 72 hrs prior to enrollment
4. Refusal of consent by the parents
5. Refusal to include by the treating team due to perceived clinical instability of the neonate
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method