CTRI/2021/04/032814Not yet recruitingNot Applicable
The effect of novel rotary file systems along with irrigation agitation technique on postoperative pain in teeth with symptomatic irreversible pulpitis : a randomized clinical trail
Dr Ravuri Varshini Meghana1 site in 1 country80 target enrollmentStarted: January 11, 2021Last updated:
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 80
- Locations
- 1
- Primary Endpoint
- Assessment of post-operative Pain scores using Visual Analog Scale
Study Overview
Brief Summary
This is a randomized, double blind, parallel group, single center trial in which we compare the effect of anatomical rotary and conventional rotary file systems along with manual dynamic agitation on post-operative pain in patients with symptomatic irreversible pulpitis will be assessed using Visual Analog Scale[VAS] at 6,24,48,and 72 hours andon 7th day.
Study Design
- Study Type
- Interventional
- Allocation
- Other
- Masking
- Participant and Outcome Assessor Blinded
Eligibility Criteria
- Ages
- 18.00 Year(s) to 50.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Patients with symptomatic irreversible pulpitis in posterior teeth.
- •Healthy patients of age group between 18-50 yrs.
- •Patients with preoperative pain scores which will vary from moderate to severe pain on a visual analog scale(VAS).
- •Patients who will have the ability to understand and to use the pain scale.
Exclusion Criteria
- •Patients with pain on percussion Patients with traumatic occlusion, severe malocclusion Teeth with calcified canals Teeth with periapical radiolucency Teeth with root resorption Teeth with immature open apex Patients with Re -RCT will be excluded.
- •â€¢Patients who has taken analgesic or anti-inflammatory drugs within the last 12 hour •Patients with known allergy to local anesthesia, sodium hypochlorite and chlorhexidine.
- •Presence of systemic diseases like cardiovascular disease, renal disease, bleeding disorders or any anti-coagulant use with in last month.
- •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.
Outcomes
Primary Outcomes
Assessment of post-operative Pain scores using Visual Analog Scale
Time Frame: at 6,24,48,and 72 hours and on 7th day
Secondary Outcomes
- assessing quality of life using OHIP 14 criteria(at 72 hours)
Investigators
Study Sites (1)
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