FindTrial
Sign In

To assess pain and discomfort and use measures to decrease pain during surfactant administration in premature babies

Pain assessment and management using nonpharmacological measures during surfactant administration by LISA vs INSURE technique - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/05/066746
Enrollment
44
Registered
2024-05-03
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: P220- Respiratory distress syndrome of newborn

Interventions

Control Intervention1: Nil: nil

Sponsors

Department of Neonatology Government medical College Chh Sambhajinagar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All babies of GA less than 37 weeks with diagnosis of RDS requiring surfactant therapy with either LISA or INSURE methods.

Exclusion criteria

Exclusion criteria: 1. Intubation before the study entry 2. Perinatal asphyxia 3. IVH more than grade II

Design outcomes

Primary

MeasureTime frame
To assess Pain profile during surfactant therapy with either LISA or INSURE method in preterm neonates diagnosed with RDSTimepoint: 1 Before surfactant administration 2 During laryngoscopy 3 During surfactant administration 4 After the procedure—

Secondary

MeasureTime frame
Adequacy of analgesiaTimepoint: During surfactant therapy—

Countries

India

Contacts

Public ContactJohn Biswas

Government medical college,Chh. Sambhajinagar

deshmukhls@yahoo.com9822478275

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026