Evaluation of the effect of low power laser in reducing the pain of mandibular block injection.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: General health Insensitivity to lidocaine injection No use of any analgesics, anesthesia, sedation and antidepressant for two weeks No pregnancy
Exclusion criteria
Exclusion criteria: Lack of cooperation Sensitivity to the injectable drug If for any reason during the intervention more than one injection is applied for each person Cancellation of the participants Very high and low pain threshold
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Measurement of pain during injection of mandibular alveolar nerve block. Timepoint: Start of study and 14 days after intervention. Method of measurement: The method of measuring pain intensity is the use of a visual analog scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Kermanshah University of Medical Sciences