Effect of serum on the complications of third Molar surgery

Phase 3

• Conditions: Mandibular third molar surgery.; Supernumerary teeth; K00.1

• Registration Number: IRCT20191127045516N3
• Lead Sponsor: Kermanshah 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 2021

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 300

Inclusion Criteria

Patients undergoing mandibular third molar surgery
They should be in the moderate surgical group.
The existence of a third mandibular molar, the occlusion of which has been confirmed by panoramic radiography.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Immediately, 2 and 7 days after surgery. Method of measurement: Visual Analogue Scale (VAS).;Inflation. Timepoint: Immediately, 2 and 7 days after surgery. Method of measurement: self report.