None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with good health in the age group of 20-70 years. Patients with symptomatic reversible pulpitis with deep dentinal caries. Patients with remaining dentin thickness at least 1-1.5mm on radiograph. Patients with preoperative pain score greater than 3 as measured on VAS scale.
Exclusion criteria
Exclusion criteria: Individuals with systemic and mental illness. Individuals with pain from multiple soft tissue or hard tissue sites. Pregnant and lactating mothers. Individuals who have taken short acting systemic or topical analgesics within 120 minutes before the dental visit or any long-acting systemic analgesics within 240 minutes before the dental visit. Presence of chronic endodontic lesions in relation to the tooth.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluvate the analgesic effect during administration of acmella oleracea gel and low level laser therapy.Timepoint: Evaluvate the analgesic effect during administration of acmella oleracea gel and low level laser therapy within 120 minutes of application | — |
Secondary
| Measure | Time frame |
|---|---|
| Intergroup comparison of analgesic effectTimepoint: compare the analgesic effect within 40 minutes | — |
Countries
India
Contacts
Coorg Institute of dental sciences