Condition 1: Trismus. Condition 2: Pain. Condition 3: Swelling. Condition 4: Total analgesic drug consumption. Cramp and spasm Pain, unspecified Edema, not elsewhere classified Other nonsteroidal anti-inflammatory drugs [NSAID]
Conditions
Interventions
Intervention 1: Intervention group:In first group red laser(with the wavelength of 660 nm and the power of 6 joules per square centimeter)is applied extraorally on 2 occasions, once 30 minutes before
2 –, lower middle region
3 –, upper middle region
and 4 –, upper region (near the insertion of the zygomatic arch). The laser will be applied for 7 minutes at each point. Intervention 2: Intervention group: In the second group infra red laser(with th
and 4 –, upper region (near the insertion of the zygomatic arch).The laser will be applied for 5 minutes at each point. Intervention 3: Control group: Placebo laser(off laser) is applied extraorally o
and 4 –, upper region (near the insertion of the zygomatic arch).
Sponsors
Tabriz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: Patients admitted to the dental clinic who require the removal of impacted lower 3rd molar Patients who have impacted lower 3rd molar with grade lllB or IIIC surgical difficulty according to Pell-Gregory classification Patients who have mesioangular impacted lower 3rd molar Patients without any systemic disease
Exclusion criteria
Exclusion criteria: Patients with distoangular or vertical impacted lower 3rd molar Soft tissue impaction of the lower 3rd molar Hypersensitivity to local anesthetics Patients with systemic disease Local infection Blood dyscrasias Patients with a history of gastric ulcer or patients who are currently suffering from a gastric ulcer Cardiovascular condition Pregnancy Lactation Patients who have used analgesic or anti inflammatory drugs 24 hours prior surgery Surgical procedures taking longer than 20 minutes
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: Day 2 post-operation, day 7 post-operation. Method of measurement: Visual analog scale (asking from patient, scoring from 1 to 10).;Swelling. Timepoint: Pre-operation, day 2 post-operation, day 7 post-operation. Method of measurement: Measuring 3 parameters: 1-tragus-labial commissure distance, 2- Lateral canthus of eye-mandibular angle distance, 3-tragus–pogonion distance.;Trismus. Timepoint: Pre-operation, day 2 post-operation, day 7 post-operation. Method of measurement: Measuring the maximum space between central incisors of maxilla and mandible( in millimeter). | — |
Secondary
| Measure | Time frame |
|---|---|
| Number of pain relief tablets taken. Timepoint: Day 2 post-operation, day 7 post-operation. Method of measurement: Asking the patient. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactJavad Yazdani
Tabriz University of Medical Sciences
Outcome results
None listed