A clinical trial to study the efficacy of two rotary file systems ,Protaper Gold and XP EndoShaper in patients with symptomatic irreversible pulpitis.
- Conditions
- Health Condition 1: K040- Pulpitis
- Registration Number
- CTRI/2021/07/035179
- Lead Sponsor
- Dr y sushmita
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.patients with symptomatic irreversible pulpitis with apical periodontitis
2. Patients of age group between 18-50 years.
3.Patients who will show prolonged response even after the removal of stimulus.
4.Patients will be included in the study after evaluation of electric pulp test response
5.Patient who has the ability to understand OHIP-14 and pain questionnaires will be provided informed consent for endodontic treatment
1.Patients with immature teeth, sinus tract, periapical abscess or
facial cellulitis.
2.Patients with generalised attrition.
3.Patients with Re -RCT will be excluded.
4.Patient with known allergies, or any contra-indication to opioid or
non-opioid analgesics including aspirin or NSAIDs.
5.Patients with known allergy to local anaesthesia, sodium
hypochlorite and chlorhexidine.
6.Presence of systemic diseases like cardiovascular disease, renal
disease, bleeding disorders or any anti-coagulant use with in last
month.
7.Pregnant and lactating mothers.
8.Patients under pain medication for dental or any other illness within
24 hours.
9.Patients who are unable or unwilling to complete the OHIP-14 and
pain questionnaires.
10.Patients who are unwilling to sign consent for endodontic treatment
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method