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Analgesic Properties of Oral Sucrose During Immunizations

NCT00446875 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 98

Last updated 2019-02-15

No results posted yet for this study

Summary

The purpose of this study is to examine the analgesic properties of oral sucrose during routine immunizations. Hypothesis: Oral sucrose solution and maternal contact will significantly decrease the objective measures of acute pain during routine immunizations.

Conditions

  • Procedural Pain

Interventions

OTHER

Administration of oral Sucrose

Participants received oral sucrose 2 minutes prior to the combind DTaP, IPV, and Hep B vaccine.

OTHER

Administration of oral Placebo

Participants received Placebo 2 minutes prior to the combind DTaP, IPV, and Hep B vaccine.

Sponsors & Collaborators

  • Milton S. Hershey Medical Center

    lead OTHER

Principal Investigators

  • Linda A Hatfield, PhD · The Penn State University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
3 Months
Max Age
11 Months
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-01-31
Primary Completion
2008-05-19
Completion
2008-05-19

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00446875 on ClinicalTrials.gov