We updated the design of this site on September 25th. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

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

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00232895
First Posted: October 5, 2005
Last Update Posted: March 28, 2007
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Institute of Child Health
  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
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

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   1 Year to 7 Years   (Child)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • ASA 1 or 2 requiring intravenous general anaesthetic

Exclusion Criteria:

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): 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

ClinicalTrials.gov Identifier: NCT00232895     History of Changes
Other Study ID Numbers: 02AR36
First Submitted: October 4, 2005
First Posted: October 5, 2005
Last Update Posted: March 28, 2007
Last Verified: March 2007

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


To Top