Health Condition 1: K029- Dental caries, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients having pain in mandibular molars due to carious exposure [pain corresponding to i50-100 mm on the VAS], delayed response to pulp sensibility tests, no peri-apical widening on radiographs, vital pulp on entering pulp chamber, normal healthy patient who can comprehend the pain scale etc.
Exclusion criteria
Exclusion criteria: Patients not willing to participate. Subjects with respiratory disease, allergy to local anesthetic solution and on pain-relieving medications at least 12 hours before the enrollment in study will be excluded from the study. Moreover, subjects in which teeth with intra-oral or extra-oral swelling, fused or extra root, gingival or periodontal inflammation will be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary objective of this double-blind, prospective, randomized controlled clinical trial will be to evaluate the effect of LLLT on LI4 acupoint in the success of IANB in mandibular molar teeth with SIP.Timepoint: Pre-operatively and during access opening | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcome will be to evaluate change in the heart rate following application of laser.Timepoint: Before and after application of laser | — |
Countries
India
Contacts
Department of Dentistry, AIIMS Nagpur