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Clinical Trials/NCT00847028
NCT00847028
Unknown
Not Applicable

Oral Glucose Solution as Pain Relief in Newborns: Results of a Clinical Trial

Universiteit Antwerpen1 site in 1 country304 target enrollmentNovember 2007
ConditionsPain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain
Sponsor
Universiteit Antwerpen
Enrollment
304
Locations
1
Primary Endpoint
Pain after venipuncture measured by the Leuven pain scale for newborns
Last Updated
17 years ago

Overview

Brief Summary

This study investigates which concentration of glucose is most effective in reducing pain for venipuncture in the newborn.

Detailed Description

This double-blind clinical trial is conducted on a maternity and newborn (N\*) ward. Each time, during at least one month, one of the four selected solutions (glucose 10%, 20%, 30% and placebo) will be administered orally, 2 minutes prior to the venipuncture. The pain from the skin puncture will be scored using a validated pain scale (the "Leuven" pain scale).

Registry
clinicaltrials.gov
Start Date
November 2007
End Date
April 2009
Last Updated
17 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Pain after venipuncture measured by the Leuven pain scale for newborns

Time Frame: solution administration- waiting for 2 minutes-then venipuncture and immediate pain scoring

Secondary Outcomes

  • difference in heart rhythm(heart rhythm measured before painful procedure - heart rythm after venipuncture compared to baseline measurement)

Study Sites (1)

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