A clinical trail to evaluate the pain after root canal treatment by two diiferent rotary systems
- Conditions
- Health Condition 1: null- Asymptomatic irreversible pulpitis
- Registration Number
- CTRI/2017/02/007774
- Lead Sponsor
- arayana dental college and hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 40
1.Multi rooted teeth with asymptomatic irreversible pulpitis with normal periapical radiographic appearance and periapical radiolucency less than 2mm will be scheduled for initial endodontic treatment.
2.Patients of age group between 18-50
3.Subjects who will show prolonged response even after the removal of the stimulus.
Patient who has the ability to understand the use of pain scales will be provided informed consent for endodontic treatment.
1.Patients with sinus tract, periapical abscess or facial cellulitis.
2.Patient with known allergies, or any contraindication to opioid or non-opioid analgesics including aspirin or NSAIDs.
Patients with known allergy to local anaesthesia, sodium hypochlorite and chlorhexidine. Presence of systemic diseases like cardiovascular disease, renal disease, and any bleeding disorders or anti coagulant use with in last month.
3.Pregnants and lactating mothers.
4.Patients under pain medication for any other illness.
5. Patients who are unable or unwilling to complete the pain questionnaires;
6. 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 post treatment pain evalution using visual analog scale after 8hours,12 hours,24hours,48hours,72hoursTimepoint: post treatment pain evalution using visual analog scale 8hours,12 hours,24hours,48hours,72hours
- Secondary Outcome Measures
Name Time Method post treatment pain evalution using visual analog scaleTimepoint: pain evaluation 24, 48, 72 hours after treatment