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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00232895
Other study ID # 02AR36
Secondary ID
Status Completed
Phase N/A
First received October 4, 2005
Last updated March 27, 2007
Est. completion date August 2005

Study information

Verified date March 2007
Source Institute of Child Health
Contact n/a
Is FDA regulated No
Health authority United Kingdom: Research Ethics Committee
Study type Interventional

Clinical Trial Summary

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


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date August 2005
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 1 Year to 7 Years
Eligibility Inclusion Criteria:

- ASA 1 or 2 requiring intravenous general anaesthetic

Exclusion Criteria:

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms

  • ASA 1-2 Requiring Intravenous Cannulation for General Anaesthesia

Intervention

Drug:
lipuro propofol

standard formulation propofol


Locations

Country Name City State
United Kingdom Great Ormond Street Hospital London

Sponsors (1)

Lead Sponsor Collaborator
Institute of Child Health

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary pain scores on induction of anaesthesia with propofol