Healthcare center Mariefred/Strängnäs
Mariefred, 64723, Sweden
NCT Number: NCT01802086
The aim of this intervention study is to compare the efficacy of Emla cream as a pain relief or no pain relief in connection to the first pneumococcal vaccination at the age of three months in Child health care.
Primary objective
1.Leads Emla cream as pain relief to children in connection with pneumococcal vaccination at the age of three months to lower pain scores in the use of five items; Face, Legs, Activity, Cry, Consolability (FLACC scale) as a pain measurement instrument?
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Notify Me2 month–4 month
All sexes
Interventional
Not applicable
Mariefred, 64723, Sweden
The aim of this intervention study is to compare the efficacy of Emla cream as a pain relief or no pain relief in connection to the first pneumococcal vaccination at the age of three months in Child health care.
Primary objective
Secondary objectives
Method: The study is randomised and singleblind. The study involves 72 children who are 3 months old. 36 children will receive Emla-cream and 36 children will receive placebo-cream.
This study will lead to new knowledge about Emla cream and pneumococcal vaccination. The study will give new knowledge how painful pneumococcal vaccination is for the children. If the study shows that Emla cream don´t give enough pain relief during pneumococcal vaccination more studies should be done with other pain relief.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Topical anaesthetic
Other names: Studied drug: Emla-Cream, lidocaine and prilocaine
Topical
Other names: Placebo: Miniderm cream containing 20 % glycerol, non-pharmacological agent
Time frame: Before vaccination and after vaccination, up to three minutes.
The effect of Emla cream on pain perception during pneumococcal vaccination was measured by FLACC scale that includes five items; Face, Legs, Activity, Cry, Consolability. FLACC scale i a qualitative behavioural scale used for pain assesment and has been validated for use in infants aged 2 months to 7 years. Each item (Face, Legs, Activity, Cry and Consolability) can give 0,1 or 2 points according to the description included in the FLACC scale. The total summarised pain score can range between 0-10 points. A higher pain-score indicate more pain, which means a worse outcome.
FLACC scale was measured before and after vaccination and compared between the groups (Emla-cream vs Miniderm cream).
Time frame: Before vaccination and after vaccination, up to three minutes.
Latency time to cry (scored in seconds):
Total crying time (scored in seconds):
Time frame: Before vaccination and after vaccination, up to three minutes
Heart rate before and after vaccination (beats per minute), higher values indicate more pain, a worse outcome. Min and max values are not applicable.
Time frame: Before vaccination and after vaccination, up to three minutes
Oxygen saturation before and after vaccination (0-100%), a lower value indicate more pain, a worse outcome
Beatrice Olsson Duse
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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