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Clinical Trials/ACTRN12612000385842
ACTRN12612000385842
Recruiting
Phase 2

A randomised double-blind placebo-controlled trial of the efficacy of Remifentanil for procedural pain in neonates

Dr Susan M Lord0 sites80 target enrollmentApril 4, 2012

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Pain relief for neonates undergoing insertion of a central venous catheter
Sponsor
Dr Susan M Lord
Enrollment
80
Status
Recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 4, 2012
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Dr Susan M Lord

Eligibility Criteria

Inclusion Criteria

  • Medically stable neonates
  • Inpatient in JHCH NICU Level 3 Nursery
  • Require insertion of a central venous catheter for their medical care
  • 24–44 weeks corrected gestational age at the time of procedure

Exclusion Criteria

  • Prior participation in this study (an infant can only participate once)
  • Major congenital anomalies
  • Severe hypoxic ischaemic encephalopathy
  • Current clinical seizures
  • Concomitant muscle relaxant
  • Emergency central line insertions
  • Lack of peripheral venous access for administration of study drug

Outcomes

Primary Outcomes

Not specified

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