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Comparative analysis of two flap designs for the extraction of impacted mandibular horizontal third molars: a multicenter randomized control trial

Phase 2
Conditions
impacted mandibular horizontal third molars
Registration Number
JPRN-UMIN000045413
Lead Sponsor
Omura Municipal Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
188
Inclusion Criteria

Not provided

Exclusion Criteria

(1) deficiency of the mandibular second molars; (2) taking an anticancer drug, an immunosuppressive drug, or an antithrombotic drug; and (3) with a systemic disease that prevents surgery.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The primary endpoint of the study was the difference in the postoperative complications (postoperative pain, hemorrhage, paralysis of the inferior dental nerve, dry socket, and infection) between mEF and TF.
Secondary Outcome Measures
NameTimeMethod
The secondary endpoint of the study was the difference in the operation time.
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