evaluation of decreasing pain of impacted wisdom teeth

Not Applicable

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

• Registration Number: IRCT20180702040302N1
• Lead Sponsor: arestan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 11 September 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 64

Inclusion Criteria

Impacted mandibular third molar
Third molar without caries
Third molar without a pericoronitis
A lack of vision of the impacted molar with the eye
An impacted molar that requires surgery to remove the need for piece of bone and teeth

Exclusion Criteria

Having a history of disease
History of digestive diseases
History of systemic diseases such as diabetes, kidney failure, liver failure
History of allergy to aspirin and its similar compounds
Patients with a history of addiction
No-referral
Non-response of the phone for any reason
Incidence of severe complications and patient death,
Use of drugs with anti-pain and anti-inflammatory properties that interfere with NSAIDs.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain intensity. Timepoint: 2,4,6,6,8, 12,24,72 hours after surgery. Method of measurement: Standard questionnaire.