None listed
Conditions
Interventions
Intervention1: Group 1: Prednisolone group
Subgroup 1A: Oral
: Subgroup 1A: Oral 40 mg prednisolone tablet will be given half an hour before the start of procedure.
Intervention2: Group 1: Prednisol
Sponsors
Dr Kokat Suhasini
Eligibility
Inclusion criteria
Inclusion criteria: 1.Systemically healthy patients (ASA I /II). 2.Patients who required endodontic treatment in lower teeth. 3.Vital teeth with no history of root canal therapy. 4.Patients who had tooth with clinical diagnosis of irreversible pulpitis. 5.Volunteers who suffered from moderate or severe pain. 6.Volunteers who signed a human subject committee approved consent form.
Exclusion criteria
Exclusion criteria: 1.Pregnant or lactating patients. 2.Patients who had taken analgesic or anti-inflammatory drugs within last 8hrs. 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 |
|---|---|
| All drugs used, decreases intra and postoperative painTimepoint: 2 hrs to 48 hrs | — |
Secondary
| Measure | Time frame |
|---|---|
| All drugs used, decreases postoperative painTimepoint: 6, 12 ,24 hrs | — |
Countries
India
Contacts
Public ContactDr K Shekar
Sri Sai College of Dental Surgery
Outcome results
None listed