Preventing procedural pain in preterm infants during Retinopathy of Prematurity screening.
Phase 3
- Conditions
- Health Condition 1: H36- Retinal disorders in diseases classified elsewhere
- Registration Number
- CTRI/2024/04/065937
- Lead Sponsor
- DR MOUNIKA B
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Neonates who will be undergoing ROP screening as per ILROP-3 recommendation for the first time.
Exclusion Criteria
1. Infants with IVH 3 or more
2. Infants on a mechanical ventilator, inotropes, sedatives
3. Infants who underwent any surgery
4. Major congenital anomalies - cardiac, neurological, facial palsy
5. Those infants whose mothers will not be available during the intervention
6. Infants whose parents do not consent to participate in the trial
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method