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Tissue adhesives for surgical wound closures

Not Applicable
Conditions
Impacted teeth.
embedded and impacted teeth with abnormal position of such teeth or adjacent teeth
Registration Number
IRCT2015050722139N1
Lead Sponsor
Vice chancellor for research, Ahvaz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
12
Inclusion Criteria

-After taking panoramic radiography patients with impacted 3rd molar with mesioangular or vertical impaction, vertical class c pell & gregory and anterior posterior class 2 pell & gregory impaction were selected.
-Patients must be younger than 25 years old
-No systemic disease,no wound healing disruptive disease,no diabetes, no bleeding disorders
-No history of anticoagulant medicines, no use of immunosuppressant drugs.
-No history of smoking and drinking
-No decays on 2nd molar

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: 1,2,3,5,7 days after surgery. Method of measurement: with pain visual analog scale questionnaire.;Bleeding. Timepoint: 1,2,3 days after surgery. Method of measurement: with bleeding questionnaire.;Wound healing. Timepoint: first and second weeks after surgery. Method of measurement: oral and maxillofacial surgeon's view.
Secondary Outcome Measures
NameTimeMethod
Patient comfort. Timepoint: first week after surgery. Method of measurement: according to patients' reports.;Sensitivity of soft tissue. Timepoint: first and second weeks after surgery. Method of measurement: evaluated by oral and maxillofacial surgeon.
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