None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with good health in the age group of 20-40 years. Patients with symptomatic irreversible pulpitis of maxillary molars. Patients with preoperative pain score greater than 54mm as measured on HP-VAS scale.
Exclusion criteria
Exclusion criteria: Individuals with systemic and mental illness. Individuals with known allergy or contraindication to lignocaine. Pregnant and lactating mothers. Individuals who have taken analgesics 12hrs before endodontic procedure. Individuals under barbiturates and benzodiazepine medication. Presence of chronic endodontic lesions in relation to the tooth.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluate the onset, anesthetic efficacy and injection pain during administration of cold anesthesia and photobiomodulation.Timepoint: Evaluate the onset, anesthetic efficacy and injection pain during administration of cold local anesthesia and photobiomdulation at the baseline. | — |
Secondary
| Measure | Time frame |
|---|---|
| Intergroup comparison of the effects of the anesthesia.Timepoint: Compare the effect of anesthesia in males & females at the baseline. | — |
Countries
India
Contacts
Coorg institute of dental sciences