To evaluate the efficacy of an ultrasonic irritant activating system and a diode laser on the root canal treatment pain experienced when used during the root canal treatment.
Not Applicable
Completed
- Conditions
- Health Condition 1: K041- Necrosis of pulp
- Registration Number
- CTRI/2022/01/039304
- Lead Sponsor
- Dr D Y Patil Dental College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 67
Inclusion Criteria
Patients with symptomatic necrosed teeth of singled rooted teeth needing a primary endodontic treatment having periapical radiolucency not more than 2mm.
Exclusion Criteria
a)Patients with systematic diseases or allergic reactions
b)Patients who are on medication.
c)Previous root canal treatment
d)Swelling or sinus tract
e)Severe periodontal disease
f)The presence of periodontal pockets more than 3 mm in the corresponding tooth
g)Periapical radiolucency of not more than 2mm
h)Teeth having calcified root
i)Teeth with immature apex
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Post operative painTimepoint: after 24 hours, 48 hours and 7 days
- Secondary Outcome Measures
Name Time Method not applicableTimepoint: not applicable