evaluation of decreasing pain of impacted wisdom teeth

Not Applicable

• Conditions: pain control.; F45.4 Persistent somatoform pain disorder; Chapter V

• Registration Number: IRCT2014113020158N1
• Lead Sponsor: Tehran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 180

Inclusion Criteria

Inclusion Criterai: impcated wisdom teeth; healthy medical history; no gastrointestinal ulcer treatment in 30days ago; no analgesic consumption in 24hours ago; no drugs addiction; no pregnancy and breastfeeding; no drugs sensitivity( Analgesics ,Non-steroidal anti-inflammatory drug commonly used, Cyclooxygenase-2 inhibitors) ; no nasal polyps; no bronchospasm and angioedema.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain intensity. Timepoint: 2,4,6,10,16,24 hours after surgery. Method of measurement: standard questionnaire.