Evaluation of Safety and Efficacy of Remifentanil in Pediatric Population

Infant, Preterm Clinical Trial

Official title:
Evaluation of Safety and Efficacy of Remifentanil in Preterm Infant

Status Completed

Clinical Trial Summary

The purpose of this study is to evaluate safety and efficacy of continuous infusion of remifentanil in preterm infant with mechanical ventilator for control of procedural pain using two different dosage of remifentanil.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Supportive Care

Related Conditions & MeSH terms

Infant, Preterm

Clinical Trial Details

NCT number	NCT01477892
Study type	Interventional
Source	Seoul National University Hospital
Contact
Status	Completed
Phase	Phase 1/Phase 2
Start date	December 2011
Completion date	April 2012

View Details

See also
	Status	Clinical Trial	Phase
	Completed	`NCT01389882` - Randomized Crossover Study of Neurally Adjusted Ventilatory Assist (NAVA) in Preterm Infants	Phase 2
	Completed	`NCT02482012` - Minor Increase Over Minimal Risk Research in NICU	N/A