MedPath

se of analgesics in pain reduction in childre

Phase 2
Conditions
Pain control during pulptherapy.
Registration Number
IRCT2014111017935N3
Lead Sponsor
Vice Chancellor for Research of Shahid Sadoughi University of Medical Sciences of Yazd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
75
Inclusion Criteria

children ages 6–12, who has primary maxillary molar spontaneous pain; no history of any systemic disease (renal, liver or digestion diseases); no history of prolonged bleeding; no history of platelet disorders; no history of hypersensitivity or allergic reactions to analgesics or any of the drugs tested.
Exclusion criteria: Patients taking analgesics within 5 hours prior to the dental procedure; uncooperative and anxious children.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain during pulp therapy. Timepoint: Right after pulp therapy. Method of measurement: Five face Visual Scale.
Secondary Outcome Measures
NameTimeMethod
Severity of Pain. Timepoint: Right after pulp therapy. Method of measurement: Five face Visual Scale.
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