Pain of Injection of Lipuro Propofol in Children Aged 1-7 Years

This study has been completed.
Sponsor:
Information provided by:
Institute of Child Health
ClinicalTrials.gov Identifier:
NCT00232895
First received: October 4, 2005
Last updated: March 27, 2007
Last verified: March 2007
  Purpose

Randomised controlled trial of pain of injection of lipuro in children age 1-7 versus the pain of injection of the standard formulation


Condition Intervention
ASA 1-2 Requiring Intravenous Cannulation for General Anaesthesia
Drug: lipuro propofol
Drug: standard formulation propofol

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double-Blind
Primary Purpose: Treatment

Resource links provided by NLM:


Further study details as provided by Institute of Child Health:

Primary Outcome Measures:
  • pain scores on induction of anaesthesia with propofol

Estimated Study Completion Date: August 2005
  Eligibility

Ages Eligible for Study:   1 Year to 7 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • ASA 1 or 2 requiring intravenous general anaesthetic

Exclusion Criteria:

-

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00232895

Locations
United Kingdom
Great Ormond Street Hospital
London, United Kingdom, WC1N 1EH
Sponsors and Collaborators
Institute of Child Health
Investigators
Principal Investigator: Mark Thomas, Dr Great Ormond Street Hospital
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00232895     History of Changes
Other Study ID Numbers: 02AR36
Study First Received: October 4, 2005
Last Updated: March 27, 2007
Health Authority: United Kingdom: Research Ethics Committee

Additional relevant MeSH terms:
Propofol
Anesthetics, Intravenous
Anesthetics, General
Anesthetics
Central Nervous System Depressants
Physiological Effects of Drugs
Pharmacologic Actions
Central Nervous System Agents
Therapeutic Uses
Hypnotics and Sedatives

ClinicalTrials.gov processed this record on April 22, 2014