Trismus. -
Conditions
Interventions
Intervention 1: Intervention group: patients in LLLT group had their operation side, treated with an 810 nm, infrared laser irradiation, intraorally 1 cm from the target tissue 10 min after surgery. I
Treatment - Devices
Placebo
Intervention group: patients in LLLT group had their operation side, treated with an 810 nm, infrared laser irradiation, intraorally 1 cm from the target tissue 10 min after surgery.
Control group: Received routine recommendation. In the placebo group the handpiece was inserted into the operative side intraorally but laser was not activated.
Sponsors
Faculty of Dentistry, Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
19 Years to 29 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Patients with unilateral impacted lower Third molar and no systemic problem and also not used any analgesic, antibiotic, corticosteroid, and sedative drug at least for fifteen days before surgery were registered at the surgery department of faculty of dentistry of Tehran university of Medical science. Exclusion criteria: Low compliant patients Not attending at the expected time of measurement.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: Before surgery-48 h after surgery-7 days after surgery. Method of measurement: Using VAS. | — |
Secondary
| Measure | Time frame |
|---|---|
| Trismus. Timepoint: Before surgery-48 h after surgery-7 days after surgery. Method of measurement: Using a rule that measure intra incisal.mm. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSheida Kordi
Faculty of dentistry
Outcome results
None listed