Correlation between complications associated with impacted mandibular third molar surgery and amniotic membrane.
Conditions
Interventions
Intervention 1: In this study, side of mandible in which amniotic membrane is applied, is considered treatment group and would be selected randomly for each patient. Surgical removal of contralateral
Treatment - Other
In this study, side of mandible in which amniotic membrane is applied, is considered treatment group and would be selected randomly for each patient. Surgical removal of contralateral wisdom tooth wou
Contralateral side is considered control.
Sponsors
Hamadan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
16 Years to 64 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: taking no medications and drugs; healthy patients with ASA 1 category; lack of allergy to local anesthesia; having bilateral mandibular third molar with similar impaction Exclusion criteria: poor oral hygiene; hypersensitivity to amniotic membrane; smoking and alcohol abuse; pregnant and lactating mothers
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: days 2 , 5 , 8. Method of measurement: VAS scale.;Swelling. Timepoint: days 2 , 5 , 8. Method of measurement: Sum of 3 distances: 1- tragus to oral commisure; 2- lateral canthus to mandibular angle; 3- tragus to pogonion.;Trismus. Timepoint: days 2 , 5 , 8. Method of measurement: Maximum opening measured between upper and lower incisors. | — |
Secondary
| Measure | Time frame |
|---|---|
| Patient satisfaction. Timepoint: days 2, 5, 8. Method of measurement: based on planned scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactOmid Soltaninia
Dental School
Outcome results
None listed