Randomized control trial to find the effectiveness of three disinfection technique in a single visitendodontic treatment of a multi - rooted non-vital tooth & find the incidence of in intolerable painover a period of three days resulting in treatment failure.

Phase 4

• Conditions: Health Condition 1: K041- Necrosis of pulp

• Registration Number: CTRI/2023/02/049559
• Lead Sponsor: Min of Def DRDO

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

• Status: Open to Recruitment
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

Multirooted tooth with a diagnosis of pulp necrosis, showing apical periodontitis (1mm-2mm) as confirmed by radiovisiography

- No spontaneous acute pain /pus discharge

-No contributory medical history

Exclusion Criteria

- Medically compromised patient

-Teeth with pus discharge

-Anatomic variations

-Patients not on analgesics or sedative medication prior to

root canal therapy

-Teeth without sinus tract

-Teeth with periapical radiolucency exceeding 3 mm × 3 mm in size

Study & Design

• Study Type: PMS
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Incidence of Post operative pain that may result in treatment failureTimepoint: evaluation after day 1, day 2 day 3

Secondary Outcome Measures

Name	Time	Method
Moderate to mild pain postoperative which is managed with analgesics is considered to be treatment success .Timepoint: evaluation after day 1,day 2, day3