Effect of Ascorbic acid on postendodontic pain.
Phase 4
- Conditions
- Health Condition 1: K040- Pulpitis
- Registration Number
- CTRI/2024/07/071647
- Lead Sponsor
- Dr Shahnaz
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Healthy patients having a tooth with symptomatic irreversible pulpitis and normal periapical radiographic appearance.
Exclusion Criteria
Presence of systemic disorders, a sensitivity to lidocaine with 1:80,000 epinephrine or a history of gastrointestinal ulcers, lactation, pregnancy, using any type of analgesic medication in the preceding 12 hours before the treatment, having a tooth not suitable for restoration, and having a full crown
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Success of preoperative ascorbic acid in reducing post-endodontic pain post-operatively after endodontic treatment.Timepoint: 4hrs, 8 hrs, 12 hrs, 24 hrs and 48 hrs postoperatively
- Secondary Outcome Measures
Name Time Method Compare the effects of ascorbic acid & placebo on post-endodontic pain reduction after endodontic treatment.Timepoint: 4 hrs 8 hrs 12 hrs 24 hrs & 48 hrs