IRCT2014111017935N3CompletedPhase 2
Comparison of pre-emptive ibuprofen, acetaminophen, and placebo administration in reducing pain during upper primary molar pulp therapy
Vice Chancellor for Research of Shahid Sadoughi University of Medical Sciences of Yazd0 sites75 target enrollmentStarted: TBDLast updated:
Conditions
Trial Snapshot
- Phase
- Phase 2
- Status
- Completed
- Sponsor
- Enrollment
- 75
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 6 years to 10 years (—)
- Sex
- All
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
Investigators
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