Evaluating the Effectiveness of Red and Infrared Low Level laser Therapy on Pain Control after Removal of Impacted Wisdom Teeth
- Conditions
- Condition 1: Trismus. Condition 2: Pain. Condition 3: Swelling. Condition 4: Total analgesic drug consumption.Cramp and spasmPain, unspecifiedEdema, not elsewhere classifiedOther nonsteroidal anti-inflammatory drugs [NSAID]R25.2Y45.3
- Registration Number
- IRCT20110420006239N2
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 30
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
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
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method umber of pain relief tablets taken. Timepoint: Day 2 post-operation, day 7 post-operation. Method of measurement: Asking the patient.