A clinical trial to study the effects of two drugs, Dexamethasone and Triamcinolone Acetonide on Post-Operative Pain after Root Canal Treatment of Teeth with Irreversible Pulpitis
Not Applicable
Completed
- Conditions
- Health Condition 1: K040- Pulpitis
- Registration Number
- CTRI/2023/03/050856
- Lead Sponsor
- DR PARI ANAND
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
•Healthy adults aged 18-50 years of age with symptomatic irreversible pulpitis.
•Patients with good general health and no chronic systemic diseases.
•Patients with a radiographically normal periapical region
Exclusion Criteria
•Teeth with periapical pathology, abscess, calcified canals or aberrant anatomy.
•Patients with History of allergy to Local anesthesia or any other experimental drugs.
•Patients with systemic disorders, pregnant and breastfeeding mothers and any conditions that contradict use of steroids.
•Patients with use of analgesics or anti-inflammatory drugs 12 hours prior to the procedure.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method post operative pain using Heft-Parker visual analogue scale (HP VAS)Timepoint: PRE-OP, POST-OP AFTER 6HRS, 12HRS, 24HRS,48HRS AND 72 HRS.
- Secondary Outcome Measures
Name Time Method POST OPERATIVE PAIN USING Heft-Parker visual analogue scale (HP VAS)Timepoint: PRE-OP,POST-OP AFTER 6HRS, 12HRS,24HRS,48HRS, 72 HRS