Study of the efficacy of Bio-C Sealer in endodontic retreatment.
Recruiting
- Conditions
- apical periodontitis
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
- persons who are at least 18 years of age at the time of obtaining consent
- who have given their written consent to participate in the study
- who are able to visit the clinic for treatment and follow-up
- who have had periapical bone resorption confirmed by dental radiographs prior to treatment
- those who have undergone re-root canal treatment
- whose clinical symptoms have resolved after root canal treatment and the results of the root canal bacterial culture test have been confirmed negative.
Exclusion Criteria
- those with severe clenching of the teeth (clenching and bruxism)
- those with root fractures.
- those with periodontal-endodontic or endodontic-periodontal lesions.
- those whose teeth under study have undergone perforation
- persons with a history of hypersensitivity, such as rashes or dermatitis, to chemical substances, including raw materials of the material under study
- women who are pregnant or possibly pregnant, lactating or wishing to become pregnant
- who are participating or intend to participate in other clinical research studies during the period of their participation in this study
- is deemed to interfere with, limit or confound the evaluation specific to the clinical research plan
- the principal investigator(s) directly involved in this or any other clinical research, or any employee of the implementing healthcare organisation, or any family member of the principal investigator(s)
- those whose clinical symptoms (spontaneous pain, bruxism, gingival swelling or redness, fistula) have not resolved despite standard root canal treatment
- those whose clinical symptoms disappear after root canal treatment but the results of the root canal bacterial culture test do not become negative for more than six months
- who have previously been enrolled in this study
- who have periapical bone resorption contiguous to the root apex of multiple teeth on pre-treatment dental radiographs
Study & Design
- Study Type
- Interventional
- Study Design
- single assignment
- Primary Outcome Measures
Name Time Method Percentage of patients with reduced or eliminated periapical bone defect image area Calculated from dental radiographs images
- Secondary Outcome Measures
Name Time Method