Assessment of postoperative pain after using two root canal sealers along with irrigating needles in symptomatic irreversible pulpitis mandibular molars - A clinical trial
- Conditions
- Health Condition 1: K040- Pulpitis
- Registration Number
- CTRI/2023/05/053313
- Lead Sponsor
- YASMEEN MOHAMMED AZEEM
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
a.Patients with symptomatic irreversible pulpitis (mandibular molar).
b.Healthy patients of age group between 18-55 yrs.
c.Patients with preoperative pain scores which will vary from moderate to severe pain on a visual analog scale (VAS).
d.Patients who will have the ability to understand and to use the pain scale.
•Patients with any uncontrolled systemic diseases.
•Retreatments of root canals.
•Teeth with immatureopen apex.
•Patients who initiated root canal treatment in other clinics.
•Patients who has taken analgesic or anti-inflammatory drugs within the last 12 hours.
•Patients with known allergy to local anaesthesia, sodium hypochlorite and chlorhexidine.
•Pregnant and lactating mothers.
•Patients who are unable or unwilling to complete the pain questionnaires.
•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