Health Condition 1: K040- Pulpitis
Conditions
Interventions
Intervention1: Control group - Placebo.: Placebo - a sugar coated tablet
Intervention2: Intervention agent - sublingual tablet of wheatgrass: 500mg
route of administration - sublingual
duration of i
Sponsors
SabahS
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients above 18 to 40 years. 2) Symptomatic irreversible pulpitis / Apical periodontitis patients in mandibular molars. 3) Pain value - according to NPRS scale of score of five or more. 4) No significant medical problems.
Exclusion criteria
Exclusion criteria: 1) Teeth with previous endodontic treatment, periapical pathology. 2) Hot tooth. 3) Analgesic ingestion within the last 4 hours. 4) History of any allergic reaction to NSAIDs. 5) Patients with neuralgic pain disorders. 6) Patients on anti-coagulants. 7) Pregnant and lactating women. 8) Patients with hypoglycemia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcome of this study is to evaluate the analgesic effect of sublingual oral medication of wheatgrass (tablet form) on pain control for patients suffering with irreversible pulpitis.Timepoint: 30 mins after drug administration. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcome of this study is to comparatively evaluate the analgesic effect of sublingual oral medication of wheatgrass (tablet form) & NSAID drug piroxicam on pain control for patients suffering with irreversible pulpitis.Timepoint: 30 mins after drug administration. | — |
Countries
India
Contacts
Public ContactShobana K
Srm kattankulathur dental college and hospital
Outcome results
None listed