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EMLA CREAM AS PAIN RELIEF DURING PNEUMOCOCCAL VACCINATIO

Conditions
Pain relief with Emla cream during Pneumococcal vaccination.
Registration Number
EUCTR2010-021406-38-SE
Lead Sponsor
Mariefreds Vårdcentral
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Authorised-recruitment may be ongoing or finished
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Healthy children, normal birth or are born with sectio after 37 weeks of gestation and who are not admitted to the neonatal unit. Children should only have been with the PKU testing performed routinely at the hospital.

Are the trial subjects under 18? yes
Number of subjects for this age range: 72
F.1.2 Adults (18-64 years) no
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Baby delivered by vacuum extraction or forceps. Children born before gestational week 37. Children in neonatal care and subjected to other testing than PKU. Shoulder dystocia. Children susceptible to methaemoglobinaemia in glucose 6-phosphate dehydrogenase deficiency, congenital or idiopathic methemoglobinemia. Children with atopic dermatitis because the application time for Emla-plaster should be shortened to 15-30 minutes

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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