Health Condition 1: K040- Pulpitis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Age range of 18-60 years. 2.Systemically healthy patients (ASA I /II). 3.Patients who required endodontic treatment in lower teeth. 4.Vital teeth with no history of root canal therapy. 5.Patients who had tooth with clinical diagnosis of irreversible pulpitis. 6.Volunteers who suffered from moderate or severe pain. 7.Volunteers who signed a human subject committee approved consent form
Exclusion criteria
Exclusion criteria: 1. Pregnancy or lactation patients. 2.Patients who had taken analgesic or anti-inflammatory drugs within last 8hr. 3.No volunteer under 18 years of age. 4.Any endocrine or infections disease or had any systemic disease that contraindicate endodontic therapy. 5.Active site of pathosis in the area of injection. 6.Moderate to advanced periodontal disease. 7.Non vital teeth (necrosis). 8.Any known sensitivity or other adverse reactions to any of the medication or materials used in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the combination of different adjuvants in the study focus on increasing profound pulpal pain relief.Timepoint: The anesthetic solution combination would start its action from 15 minutes of administration and the duration of action would last for 4 hours . | — |
Secondary
| Measure | Time frame |
|---|---|
| the combinations would act on increasing the quality and depth of the local anesthesiaTimepoint: the duration of of local anesthetic action would last for 8 to 12 hours. | — |
Countries
India
Contacts
Sri Sai College of Dental Surgery