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Comparison of tramadol with lidocaine for circumcision procedure.

Not Applicable
Conditions
circumcision.
Routine and ritual circumcision
Registration Number
IRCT201106183468N7
Lead Sponsor
Pain Research Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Male
Target Recruitment
60
Inclusion Criteria

full physical health; age 0-5 years
Exclusion criteria: anatomical malformation; sensitivity to study drug

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: at intervention-1-5-10-20 minute after intervention. Method of measurement: CHIOPS (Children's Hospital of Eastern Ontario Pain Scale).;Total analgesic consumption. Timepoint: 24 after intervention. Method of measurement: mg/kg consumped ibuprofen.;Time to first analgesic request. Timepoint: time between intervention and first analgesic administratin. Method of measurement: minutes.
Secondary Outcome Measures
NameTimeMethod
Side effects. Timepoint: 24 hours after intervention. Method of measurement: observation.
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