A clinical Trial to study the effect of Neurophysiological Facilitation technique on the amount of oxygen in preterm babies
Not Applicable
Completed
- Conditions
- Health Condition 1: J80- Acute respiratory distress syndrome
- Registration Number
- CTRI/2019/04/018594
- Lead Sponsor
- Mitu Sethiya
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 9
Inclusion Criteria
infants in NICU with Gestational Age of 30 to 37 weeks, saturation of 85 to 95 %, respiratory rate of 30 to 60 breaths per minute, intercostal indrawing.
Exclusion Criteria
Infants in NICU with:
Uncompensated acid-base
balance, Bradycardia or Tachycardia, Cardiac arrest survivor, Untreated/ symptomatic Congenital heart disease, Post-operative cases, Diaphragmatic hernia, Laryngo-malacia, Neonates weighting less than 1000 grams.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Oxygen Saturation in PercentageTimepoint: 3 days, 2 sessions per day
- Secondary Outcome Measures
Name Time Method work of breathing using the silverman anderson scaleTimepoint: 3 days, 2 sessions per day