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A Study to compare side effects and complications during endotracheal intubation of new borns with or without using standard protocol

A comparative study on intubation associated adverse events in neonatal endotracheal intubation before and after standardised protocol with premedication

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/02/040281
Enrollment
84
Registered
2022-02-14
Start date
Unknown
Completion date
Unknown
Last updated
2022-02-21

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

Conditions

Health Condition 1: P229- Respiratory distress of newborn, unspecified

Interventions

Intervention1: Standardised Intubation Protocol With Premedication: To assess the incidence of intubation associated adverse events for neonatal intubations and to study the effectiveness of using st

Sponsors

Dr Mehta Multispecialty Hospital Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All newborn requiring intubation in NICU

Exclusion criteria

Exclusion criteria: Delivery room intubations Craniofacial anomalies

Design outcomes

Primary

MeasureTime frame
Occurrence of tracheal intubation associated adverse event Timepoint: Assessments at Baseline—

Secondary

MeasureTime frame
Time taken from decision to intubation Number of attempts and time taken for successful intubation Time to desaturation in every attempt Factors associated with adverse events such as attending person and the use of premedication Compliance to premedication Timepoint: Assessed at Baseline—

Countries

India

Contacts

Public ContactDr Anita Chrisbina J

Dr Mehta Multispecialty Hospital Pvt Ltd

drlakshmi2008@gmail.com9840211742

Outcome results

None listed

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