Single Visit Root Canal Treatment :Incidence of Postoperative Pain Using Two Different Sealers : A Randomized Clinical Trial
Trial Snapshot
- Phase
- Not Applicable
- Sponsor
- Cairo University
- Enrollment
- 68
- Primary Endpoint
- Intensity of postoperative pain
Study Overview
Brief Summary
The aim of this randomized clinical trial was to compare the potential effects of resin-based and bio ceramic sealers on the occurrence and intensity of postoperative pain in patients with asymptomatic apical periodontitis (AAP) .
Detailed Description
Reports about postoperative pain in endodontics range from 3%-58% in different studies .
Pain can be provoked by mechanical, chemical, or microbiological injuries to periodontal tissues . A number of treatment related parameters have been shown to be associated with the presence of postoperative pain, including working length (WL) estimation with an apex locator connected to every file , the number of visits , the choice of instrumentation , and the choice of root canal sealer .
Sealers placed in the root canals interfere with periodontal tissues through the apical foramina, lateral canals, or leaching and can potentially affect the healing process in the periodontium. Thus, the local inflammation caused by root canal obturation materials may result in postoperative pain. The intensity of inflammatory reactions depends on a number of different factors, including the composition of the sealer .
The use of a sealer during root canal obturation is essential for success of root canal treatment. The sealer has various functions:
- Attainment of impervious seal
- Filler for canal irregularities and minor discrepancies between the root canal wall and core-filling material Expressed through lateral or accessory canals
- Can assist in microbial control
- Act as lubricant
- Can have adhesive property to dentin
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Single (Participant)
Eligibility Criteria
- Ages
- 18 Years to 65 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Permanent teeth with fully formed apex
- •Teeth with vital pulp
- •Teeth with no periapical radiolucency
- •Patients having preoperative pain
Exclusion Criteria
- •Teeth with incompletely formed apex
- •Teeth requiring secondary endodontic treatment
- •Patients having complicating systemic disease such as diabetes, malignancy, pregnancy, central nervous system disorders, Cardiovascular system disorders, respiratory disorders, asthma patients, psychiatric disorders, immunocompromised patients,
- •Patients taking anti-inflammatory or antibiotics
- •Patients giving history of analgesic or antibiotic intake 1 week before treatment
- •Patients below 18 years of age,
- •Patients above 65 years of age
- •Patients having history of peptic ulcer or gastrointestinal bleeding,
- •Teeth having calcified canals,
- •Teeth having multiple canals or multirooted teeth,
- •Teeth affected with periodontal disease.
- •Teeth tender on percussion,
- •Teeth having procedural errors such as transportation, perforation, and missed canals
Outcomes
Primary Outcomes
Intensity of postoperative pain
Time Frame: 24th hours
Intensity of postoperative pain after using two types of sealers will be measured using a visual analog scale (VAS) after treatment
Secondary Outcomes
- intensity of postoperative pain(5th day)
Investigators
Muna Abubaker Beshir Mohamed
Principle investigator
Cairo University